HP AXIS- argentum nitricum, berberis vulgaris, iodium, kali carbonicum, natrum muriaticum, adrenalinum, cortisone aceticum, dhea

United States - English - NLM (National Library of Medicine)

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Active ingredient:
SILVER NITRATE (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A), BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U), IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4), POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D), SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698), EPINEPHRINE (UNII: YKH834O4BH) (EPINEPHRINE - UNII:YKH834O4BH), CORTISONE ACETATE (UNII: 883WKN7W8X) (CORTISONE - UNII:V27W9254FZ), PRASTERONE (UNII:
Available from:
Deseret Biologicals, Inc.
Administration route:
ORAL
Prescription type:
OTC DRUG
Therapeutic indications:
For temporary relief of symptoms related to circadian rhythm imbalances such as overuse of stimulants, anxiousness, sleep disturbances, circulatory imbalances, decreased sex drive and salt cravings.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration. For temporary relief of symptoms related to circadian rhythm imbalances such as overuse of stimulants, anxiousness, sleep disturbances, circulatory imbalances, decreased sex drive and salt cravings.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Authorization status:
unapproved homeopathic
Authorization number:
43742-1514-1

HP AXIS- argentum nitricum, berberis vulgaris, iodium, kali carbonicum, natrum muriaticum,

adrenalinum, cortisone aceticum, dhea, glandula suprarenalis suis, hypophysis suis,

hypothalamus suis, melatonin, testosterone, arsenicum album, phosphorus, proteus (vulgaris),

sepia, silicea, alloxanum, corticotropin releasing hormone, adrenocorticotrophin,

aldosterone liquid

Deseret Biologicals, Inc.

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for

safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

----------

Drug Facts:

ACTIVE INGREDIENTS:

Argentum Nitricum 6X, Berberis Vulgaris 6X, Iodium 6X, Kali Carbonicum 6X, Natrum Muriaticum

6X, 12X, 18X, 24X, 30X, Adrenalinum 6X, 12X, 18X, 24X, 30X, Cortisone Aceticum 6X, 12X, 18X,

24X, 30X, DHEA (Dehydroepiandrosterone) 6X, 12X, 18X, 24X, 30X, Glandula Suprarenalis Suis 6X,

12X, 18X, 24X, 30X, Hypophysis Suis 6X, 12X, 18X, 24X, 30X, Hypothalamus Suis 6X, 12X, 18X,

24X, 30X, Melatonin 6X, 12X, 18X, 24X, 30X, Testosterone 6X, 12X, 18X, 24X, 30X, Arsenicum

Album 12X, Phosphorus 12X, Proteus (Vulgaris) 12X, Sepia 12X, Silicea 12X, Alloxanum 18X,

Corticotropin Releasing Hormone 12C, 18C, 24C, 30C, Adrenocorticotrophin 15C, 18C, 24C, 30C,

Aldosterone 15C, 18C, 24C, 30C.

HOMEOPATHIC INDICATIONS:

For temporary relief of symptoms related to circadian rhythm imbalances such as overuse of stimulants,

anxiousness, sleep disturbances, circulatory imbalances, decreased sex drive and salt cravings.**

**These statements are based upon traditional homeopathic principles. They have not been reviewed by

the Food and Drug Administration.

WARNINGS:

Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right

away.

If pregnant or breast-feeding, ask a health professional before use.

Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right

away.

DIRECTIONS:

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician

for use in children under 12 years of age.

HOMEOPATHIC INDICATIONS:

For temporary relief of symptoms related to circadian rhythm imbalances such as overuse of stimulants,

anxiousness, sleep disturbances, circulatory imbalances, decreased sex drive and salt cravings.**

**These statements are based upon traditional homeopathic principles. They have not been reviewed by

the Food and Drug Administration.

INACTIVE INGREDIENTS:

Demineralized Water, 25% Ethanol

QUESTIONS:

Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070 www.desbio.com

PACKAGE LABEL DISPLAY:

DESBIO

NDC 43742-1514-1

HOMEOPATHIC

HP AXIS

1 FL OZ (30 ml)

HP AXIS

argentum nitricum, berberis vulgaris, iodium, kali carbonicum, natrum muriaticum, adrenalinum, cortisone aceticum,

dhea, glandula suprarenalis suis, hypophysis suis, hypothalamus suis, melatonin, testosterone, arsenicum album,

phosphorus, proteus (vulgaris), sepia, silicea, alloxanum, corticotropin releasing hormone, adrenocorticotrophin,

aldosterone liquid

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:43742-1514

Route of Administration

ORAL

DEA Sche dule

CIII

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

SILVER NITRATE (UNII: 9 5IT3W8 JZE) (SILVER CATION - UNII:57N7B0 K9 0 A)

SILVER NITRATE

6 [hp_X]

in 1 mL

BERBERIS VULGARIS RO O T BARK (UNII: 1TH8 Q20 J0 U) (BERBERIS VULGARIS

ROOT BARK - UNII:1TH8 Q20 J0 U)

BERBERIS VULGARIS

ROOT BARK

6 [hp_X]

in 1 mL

IO DINE (UNII: 9 6 79 TC0 7X4) (IODINE - UNII:9 6 79 TC0 7X4)

IODINE

6 [hp_X]

in 1 mL

PO TASSIUM CARBO NATE (UNII: BQN1B9 B9 HA) (CARBONATE ION -

UNII:7UJQ5OPE7D)

POTASSIUM CARBONATE

6 [hp_X]

in 1 mL

SO DIUM CHLO RIDE (UNII: 451W47IQ8 X) (CHLORIDE ION - UNII:Q32ZN48 6 9 8 )

SODIUM CHLORIDE

6 [hp_X]

in 1 mL

EPINEPHRINE (UNII: YKH8 34O4BH) (EPINEPHRINE - UNII:YKH8 34O4BH)

EPINEPHRINE

8 [hp_X]

in 1 mL

CO RTISO NE ACETATE (UNII: 8 8 3WKN7W8 X) (CORTISONE - UNII:V27W9 254FZ)

CORTISONE ACETATE

8 [hp_X]

in 1 mL

PRASTERO NE (UNII: 459 AG36 T1B) (PRASTERONE - UNII:459 AG36 T1B)

PRASTERONE

8 [hp_X]

in 1 mL

SUS SCRO FA ADRENAL GLAND (UNII: 39 8 IYQ16 YV) (SUS SCROFA ADRENAL GLAND

- UNII:39 8 IYQ16 YV)

SUS SCROFA ADRENAL

GLAND

8 [hp_X]

in 1 mL

SUS SCRO FA PITUITARY GLAND (UNII: L0 PFEMQ1DT) (SUS SCROFA PITUITARY

GLAND - UNII:L0 PFEMQ1DT)

SUS SCROFA PITUITARY

GLAND

8 [hp_X]

in 1 mL

SUS SCRO FA HYPO THALAMUS (UNII: N6 R0 8 56 Z79 ) (SUS SCROFA HYPOTHALAMUS

- UNII:N6 R0 8 56 Z79 )

SUS SCROFA

HYPOTHALAMUS

8 [hp_X]

in 1 mL

MELATO NIN (UNII: JL5DK9 3RCL) (MELATONIN - UNII:JL5DK9 3RCL)

MELATONIN

8 [hp_X]

in 1 mL

TESTO STERO NE (UNII: 3XMK78 S47O) (TESTOSTERONE - UNII:3XMK78 S47O)

TESTOSTERONE

8 [hp_X]

in 1 mL

ARSENIC TRIO XIDE (UNII: S7V9 2P6 7HO) (ARSENIC CATION (3+) - UNII:C9 6 6 13F5AV)

ARSENIC TRIOXIDE

12 [hp_X]

in 1 mL

PHO SPHO RUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W)

PHOSPHORUS

12 [hp_X]

in 1 mL

PRO TEUS VULGARIS (UNII: 11T9 HCO30 O) (PROTEUS VULGARIS - UNII:11T9 HCO30 O)

PROTEUS VULGARIS

12 [hp_X]

in 1 mL

SEPIA O FFICINALIS JUICE (UNII: QDL8 3WN8 C2) (SEPIA OFFICINALIS JUICE -

UNII:QDL8 3WN8 C2)

SEPIA OFFICINALIS JUICE

12 [hp_X]

in 1 mL

SILICO N DIO XIDE (UNII: ETJ7Z6 XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6 XBU4)

SILICON DIOXIDE

12 [hp_X]

in 1 mL

ALLO XAN (UNII: 6 SW5YHA5NG) (ALLOXAN - UNII:6 SW5YHA5NG)

ALLOXAN

18 [hp_X]

in 1 mL

CO RTICO RELIN (UNII: 30 5OE8 8 6 2Y) (CORTICORELIN - UNII:30 5OE8 8 6 2Y)

CORTICORELIN

12 [hp_C]

in 1 mL

CO RTICO TRO PIN (UNII: K0 U6 8 Q2TXA) (CORTICOTROPIN - UNII:K0 U6 8 Q2TXA)

CORTICOTROPIN

15 [hp_C]

in 1 mL

ALDO STERO NE (UNII: 49 6 4P6 T9 RB) (ALDOSTERONE - UNII:49 6 4P6 T9 RB)

ALDOSTERONE

15 [hp_C]

in 1 mL

Inactive Ingredients

Ingredient Name

Stre ng th

WATER (UNII: 0 59 QF0 KO0 R)

ALCO HO L (UNII: 3K9 9 58 V9 0 M)

Deseret Biologicals, Inc.

Packag ing

#

Item Code

Package Description

Marketing Start

Date

Marketing End

Date

1

NDC:43742-1514-

30 mL in 1 BOTTLE, DROPPER; Type 0 : No t a Co mbinatio n

Pro duc t

0 7/26 /20 19

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

unappro ved ho meo pathic

0 7/26 /20 19

Labeler -

Deseret Biologicals, Inc. (940741853)

Registrant -

Apotheca Company (844330915)

Establishment

Name

Ad d re s s

ID/FEI

Busine ss Ope rations

Apo the c a

Co mpany

8 44330 9 15

manufacture(43742-1514) , api manufacture(43742-1514) , label(43742-1514) , pack(43742-

1514)

Revised: 7/2019

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