NDC | 59262-351-12 |
Set ID | f3bad888-2207-4a78-abba-d3c667e30e5c |
Category | HUMAN OTC DRUG LABEL |
Packager | Similasan Corporation |
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- Active Ingredient
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- Active Ingredient
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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
- Other information
- Inactive Ingredients
- Questions?
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
DRY EYE RELIEF
belladonna 6x, euphrasia 6x, mercurius sublimatus 6x solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59262-351 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:59262-351-12 20 in 1 CARTON 07/02/2013 1 0.4 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED HOMEOPATHIC 07/02/2013 Labeler - Similasan Corporation (111566530)