ARTEMESIA ABSINTHIUM 5 SPECIAL ORDER- artemesia absinthium 5 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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Artemesia absinthium 5 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: 100 gm contains: 5g Absinthium ex herba 1X

Inactive Ingredients: Distilled water, 20% Organic grain alcohol

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. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.

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

ArtemesiaAbsinthium5SOLiquid

ARTEMESIA ABSINTHIUM 5 SPECIAL ORDER 
artemesia absinthium 5 special order liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-1260
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WORMWOOD (UNII: F84709P2XV) (WORMWOOD - UNII:F84709P2XV) WORMWOOD1 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48951-1260-360 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product09/01/2009
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic09/01/2009
Labeler - Uriel Pharmacy Inc. (043471163)
Establishment
NameAddressID/FEIBusiness Operations
Uriel Pharmacy Inc.043471163manufacture(48951-1260)

Revised: 4/2018
Document Id: 6a0eaf5e-3f0e-1d8a-e053-2991aa0aef85
Set id: b67068d4-eb75-4646-bf0e-e71535242e28
Version: 2
Effective Time: 20180417
 
Uriel Pharmacy Inc.