Label: CAREONE MAXIMUM REDNESS RELIEF EYE DROPS- glycerin, naphazoline hci liquid
- NDC Code(s): 72476-012-01
- Packager: Retail Business Services, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 January 12, 2020
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- Official Label (Printer Friendly)
- Active ingredients
- Purposes
- 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
- overuse may produce increased redness of the eye
- pupils may become enlarged temporarily
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
- CareOne Maximum Redness Relief Eye Drops 15mL
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INGREDIENTS AND APPEARANCE
CAREONE MAXIMUM REDNESS RELIEF EYE DROPS
glycerin, naphazoline hci liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72476-012 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 0.5 g in 100 mL NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D) (NAPHAZOLINE - UNII:H231GF11BV) NAPHAZOLINE HYDROCHLORIDE 0.03 g in 100 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) BORIC ACID (UNII: R57ZHV85D4) SODIUM BORATE (UNII: 91MBZ8H3QO) EDETATE DISODIUM (UNII: 7FLD91C86K) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72476-012-01 1 in 1 BOX 01/12/2020 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 01/12/2020 Labeler - Retail Business Services, LLC (967989935) Registrant - KC Pharmaceuticals, Inc. (174450460) Establishment Name Address ID/FEI Business Operations KC Pharmaceuticals, Inc. 174450460 manufacture(72476-012) , pack(72476-012) , label(72476-012)