Label: EYE DROPS- glycerin solution
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Contains inactivated NDC Code(s)
NDC Code(s): 46823-001-05 - Packager: Opto-Pharm Pte Ltd
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated March 6, 2017
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
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Warnings
For external use only
When using this product
- to avoid contamination, do not touch tip of container to any surface
- replace cap after using
- Directions
- Other informations
- Inactive ingredients
- Questions
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
EYE DROPS
glycerin solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:46823-001 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 1 g in 100 g Inactive Ingredients Ingredient Name Strength BORIC ACID (UNII: R57ZHV85D4) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) N-ACETYLCARNOSINE (UNII: 0TPN86OQIF) POTASSIUM BICARBONATE (UNII: HM5Z15LEBN) BENZYL ALCOHOL (UNII: LKG8494WBH) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:46823-001-05 10 g in 1 VIAL; Type 0: Not a Combination Product 03/06/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part346 03/06/2017 Labeler - Opto-Pharm Pte Ltd (595239682) Registrant - Opto-Pharm Pte Ltd (595239682)