Label: IRRITATED EYE- atropa belladonna and calcium sulfide and euphrasia stricta solution/ drops
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Contains inactivated NDC Code(s)
NDC Code(s): 0363-9031-11 - Packager: Walgreen Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
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 Label Information
Updated December 20, 2012
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Active Ingredient
- Purpose
- Active Ingredient
- Purpose
- Uses:
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Warnings:
- For external use only.
- Children under 2 years of age should be seen by a physician.
- Initial exacerbation of symptoms may occur.
- To avoid contamination, do not touch the tip of the container to any surface.
- Use within 30 days of opening. Expiration date only refers to unopened bottle.
- Replace cap tightly after every use.
- Contact wearers: consult physician prior to using.
- The use of this container by more than one person may spread infection.
- Do not use
- Stop use and ask a doctor if:
- Directions:
- Other Information:
- Inactive ingredients:
- Questions or comments?
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INGREDIENTS AND APPEARANCE
IRRITATED EYE
atropa belladonna and calcium sulfide and euphrasia stricta solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-9031 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA 6 [hp_X] in 10 mL EUPHRASIA STRICTA (UNII: C9642I91WL) (EUPHRASIA STRICTA - UNII:C9642I91WL) EUPHRASIA STRICTA 6 [hp_X] in 10 mL CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) CALCIUM SULFIDE 12 [hp_X] in 10 mL Inactive Ingredients Ingredient Name Strength BORIC ACID (UNII: R57ZHV85D4) WATER (UNII: 059QF0KO0R) SILVER SULFATE (UNII: 8QG6HV4ZPO) SODIUM NITRATE (UNII: 8M4L3H2ZVZ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-9031-11 1 in 1 CARTON 1 10 mL in 1 BOTTLE, DROPPER Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED HOMEOPATHIC 12/14/2012 Labeler - Walgreen Company (008965063)