ADRENALINUM pellet

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

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Active ingredient:
EPINEPHRINE (UNII: YKH834O4BH) (EPINEPHRINE - UNII:YKH834O4BH)
Available from:
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Administration route:
ORAL
Prescription type:
OTC DRUG
Therapeutic indications:
Debility Condition listed above or as directed by the physician
Authorization status:
unapproved homeopathic
Authorization number:
15631-0007-0, 15631-0007-1, 15631-0007-2, 15631-0007-3, 15631-0007-4, 15631-0007-5

ADRENALINUM- adrenalinum pellet

Rxhomeo Private Limited d.b.a. Rxhomeo, 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.

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ACTIVE INGREDIENT

ADRENALINUM HPUS 6X and higher

USES

Debility

INDICATIONS

Condition listed above or as directed by the physician

DOSAGE

Adults- Take 4 or 6 Pellets by mouth, three times daily or as suggested by physician. Children 2 years

and older- take 1/2 the adult dose.

WARNINGS

This product is to be used for self-limiting conditions

If symptoms do not improve in 4 days, or worsen, discontinue use and seek assistance of health

professional

As with any drug, if you are preganant, or nursing a baby, seek professional advice before taking this

product

Keep this and all medication out of reach of children

Do not use if capseal is broken or missing.

Close the cap tightly after use.

INACTIVE INGREDIENTS

Sucrose

STORAGE

Store in a cool dark place

QUESTIONS OR COMMENTS

www.Rxhomeo.com | 1.888.2796642 | info@rxhomeo.com

Rxhomeo, Inc 9415 Burnet Road, Suite 312, Austin, TX 78758

ADRENALINUM

adrenalinum pellet

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:156 31-0 0 0 7

Route of Administration

ORAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

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

EPINEPHRINE

6 [hp_X]

Inactive Ingredients

Ingredient Name

Stre ng th

SUCRO SE (UNII: C151H8 M554)

Packag ing

#

Item Code

Package Description

Marketing Start Date

Marketing End Date

1

NDC:156 31-0 0 0 7-0

10 0 in 1 PACKAGE; Type 0 : No t a Co mbinatio n Pro duct

0 1/0 1/20 18

2

NDC:156 31-0 0 0 7-1

20 0 in 1 PACKAGE; Type 0 : No t a Co mbinatio n Pro duct

0 1/0 1/20 18

3

NDC:156 31-0 0 0 7-2

40 0 in 1 PACKAGE; Type 0 : No t a Co mbinatio n Pro duct

0 1/0 1/20 18

4

NDC:156 31-0 0 0 7-3

750 in 1 PACKAGE; Type 0 : No t a Co mbinatio n Pro duct

0 1/0 1/20 18

5

NDC:156 31-0 0 0 7-4

250 0 in 1 PACKAGE; Type 0 : No t a Co mbinatio n Pro duct

0 1/0 1/20 18

6

NDC:156 31-0 0 0 7-5

1250 0 in 1 PACKAGE; Type 0 : No t a Co mbinatio n Pro duct

0 1/0 1/20 18

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

10 /0 2/20 15

Labeler -

Rxhomeo Private Limited d.b.a. Rxhomeo, Inc (650833994)

Rxhomeo Private Limited d.b.a. Rxhomeo, Inc

Establishment

Name

Ad d re s s

ID/FEI

Busine ss Ope rations

Rxho meo Private Limited d.b.a. Rxho meo , Inc

6 50 8 339 9 4

manufacture(156 31-0 0 0 7) , label(156 31-0 0 0 7)

Revised: 2/2020

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