Label: CLEAR VISION EYE DROPS- polyvinyl alcohol, povidone solution/ drops
- NDC Code(s): 67751-212-01
- Packager: Navajo Manufacturing Company Inc.
- 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 July 14, 2021
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients
- Uses
-
Warnings
For external use only
When using this product
- remove contact lens before using
- to avoid contamination, do not touch tip of container to any surface
- replace cap after using. Keep container tightly closed.
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
- Package Labeling
-
INGREDIENTS AND APPEARANCE
CLEAR VISION EYE DROPS
polyvinyl alcohol, povidone solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67751-212 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) (POLYVINYL ALCOHOL, UNSPECIFIED - UNII:532B59J990) POLYVINYL ALCOHOL, UNSPECIFIED 5 mg in 1 mL POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) (POVIDONE, UNSPECIFIED - UNII:FZ989GH94E) POVIDONE, UNSPECIFIED 6 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F) EDETATE DISODIUM (UNII: 7FLD91C86K) DEXTROSE (UNII: IY9XDZ35W2) SODIUM BICARBONATE (UNII: 8MDF5V39QO) SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM CITRATE (UNII: 1Q73Q2JULR) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) POTASSIUM CHLORIDE (UNII: 660YQ98I10) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67751-212-01 1 in 1 CARTON 07/14/2021 1 15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part349 07/14/2021 Labeler - Navajo Manufacturing Company Inc. (091917799) Establishment Name Address ID/FEI Business Operations Navajo Manufacturing Company Inc. 136941411 relabel(67751-212) , repack(67751-212) Establishment Name Address ID/FEI Business Operations KC Pharmaceuticals, Inc. 174450460 manufacture(67751-212) , label(67751-212)


