ARSENICUM ALBUM 6X SPECIAL ORDER liquid

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

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Active ingredient:
ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV)
Available from:
Uriel Pharmacy Inc.
Administration route:
ORAL
Prescription type:
OTC DRUG
Therapeutic indications:
Directions: FOR ORAL USE ONLY. Use: Temporary relief of headache.
Authorization status:
unapproved homeopathic
Authorization number:
48951-1335-3

ARSENICUM ALBUM 6X SPECIAL ORDER- arsenicum album 6x special order liquid

Uriel Pharmacy 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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Arsenicum album 6X Special Order

Directions: FOR ORAL USE ONLY.

Take 3-4 times daily. Ages 12 and older: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor.

Active Ingredient: Arsenicum album (White arsenic) 6X

Inactive Ingredient: Distilled water

Use: Temporary relief of headache.

KEEP OUT OF REACH OF CHILDREN.

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA

evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions

or if conditions worsen or persist. Contains traces of lactose. If pregnant or nursing, consult a doctor

before use. Do not use if safety seal is broken or missing.

REFRIGERATE AFTER OPENING.

BEST WHEN USED WITHIN 90 DAYS OF OPENING.

Questions? Call 866.642.2858 Made with care by Uriel, East Troy, WI 53120 www.urielpharmacy.com

ARSENICUM ALBUM 6X SPECIAL ORDER

arsenicum album 6x special order liquid

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:48 9 51-1335

Route of Administration

ORAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

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

ARSENIC TRIOXIDE

6 [hp_X] in 1 mL

Uriel Pharmacy Inc.

Inactive Ingredients

Ingredient Name

Stre ng th

WATER (UNII: 0 59 QF0 KO0 R)

Packag ing

#

Item Code

Package Description

Marketing Start

Date

Marketing End

Date

1

NDC:48 9 51-1335-

6 0 mL in 1 BOTTLE, DROPPER; Type 0 : No t a Co mbinatio n

Pro duc t

0 9 /0 1/20 0 9

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 9 /0 1/20 0 9

Labeler -

Uriel Pharmacy Inc. (043471163)

Establishment

Name

Ad d re s s

ID/FEI

Busine ss Ope rations

Uriel Pharmacy Inc.

0 4347116 3

ma nufa c ture (48 9 51-1335)

Revised: 11/2019

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