Label: DRY EYE RELIEF- atropa belladonna and euphrasia stricta and mercuric chloride solution/ drops
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Contains inactivated NDC Code(s)
NDC Code(s): 59262-352-01, 59262-352-13 - Packager: Similasan Corporation
- 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 November 14, 2018
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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.
- Initial exacerbation of symptoms may occur.
- Use only if single-use dropper is intact.
- To avoid contamination, do not touch the tip of the dropper to any surface. Do not reuse. Once opened, discard.
- Contact wearers: consult a physician prior to using.
- Directions
- Inactive Ingredients
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INGREDIENTS AND APPEARANCE
DRY EYE RELIEF
atropa belladonna and euphrasia stricta and mercuric chloride solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59262-352 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 0.4 mL EUPHRASIA STRICTA (UNII: C9642I91WL) (EUPHRASIA STRICTA - UNII:C9642I91WL) EUPHRASIA STRICTA 6 [hp_X] in 0.4 mL MERCURIC CHLORIDE (UNII: 53GH7MZT1R) (MERCURIC CATION - UNII:ED30FJ8Y42) MERCURIC CHLORIDE 6 [hp_X] in 0.4 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE (UNII: 5QWK665956) SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59262-352-01 270 in 1 CARTON 07/02/2013 1 0.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product 2 NDC:59262-352-13 .4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product 07/02/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED HOMEOPATHIC 07/02/2013 Labeler - Similasan Corporation (111566530) Establishment Name Address ID/FEI Business Operations International Packaging Inc 071493142 REPACK(59262-352)