Label: SODIUM CHLORIDE HYPERTONICITY- sodium chloride solution
- NDC Code(s): 69842-284-15
- Packager: CVS Pharmacy
- 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 January 25, 2021
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
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Warnings
For external use only
Do not use
▪ except under the advice and supervision of a doctor
▪ if solution changes color or becomes cloudyWhen using this product
▪ it may cause temporary burning and irritation
▪ to avoid contamination do not touch tip of container to any surface
▪ replace cap after useStop use and ask a doctor if
▪ condition worsens or persists for more than 72 hours
▪ you experience eye pain, changes in vision, continued redness or irritation of the eye - Keep out of reach of children.
- Directions
- Inactive ingredients
- Package/Label Principal Display Panel
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INGREDIENTS AND APPEARANCE
SODIUM CHLORIDE HYPERTONICITY
sodium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-284 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength sodium chloride (UNII: 451W47IQ8X) (sodium cation - UNII:LYR4M0NH37) sodium chloride 50 mg in 1 mL Inactive Ingredients Ingredient Name Strength BORIC ACID (UNII: R57ZHV85D4) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SODIUM BORATE (UNII: 91MBZ8H3QO) HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-284-15 1 in 1 CARTON 05/01/2021 1 15 mL in 1 BOTTLE; 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 05/01/2020 Labeler - CVS Pharmacy (062312574) Establishment Name Address ID/FEI Business Operations Bausch & Lomb Incorporated 079587625 MANUFACTURE(69842-284)