Label: PINK EYE REMEDY- belladonna and euphrasia and hepar sulphuris solution/ drops
-
Contains inactivated NDC Code(s)
NDC Code(s): 0363-9030-11 - Packager: Walgreen Co
- 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 August 13, 2010
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Active Ingredient
- Purpose
- Active Ingredient
- Purpose
-
Uses
According to homeopathic principles, the active ingredients in this medication temporarily relieve minor symptoms associated with viral and environmental conjunctivitis such as:
- redness of the whites of the eyes and inner eyelids
- excessive watery (clear) discharge
- sensation of grittiness
- redness and burning -
Warnings
- For external use only.
- Children under 2 years of age should be seen by a physician.
- Initial exacerbation of symptoms may occur.
- Use only if bottle seal is intact.
- 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 a physician prior to using.
- The use of this container by more than one person may spread infection.
- Keep this and all medicines out of the reach of children
- If swallowed, get medical help or contact a Poison Control Center right away. - Do Not Use
- Stop use and ask a doctor if
- Directions
- Other Information
- Inactive ingredients
- Questions?
- Prinicipal Display Panel
-
INGREDIENTS AND APPEARANCE
PINK EYE REMEDY
belladonna and euphrasia and hepar sulphuris solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-9030 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 CATION - UNII:2M83C4R6ZB) 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:0363-9030-11 10 mL in 1 BOTTLE, DROPPER Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED HOMEOPATHIC 12/01/2007 Labeler - Walgreen Co (008965063)
