Label: SODIUM CHLORIDE ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 54868-4698-0 - Packager: Physicians Total Care, Inc.
- This is a repackaged label.
- Source NDC Code(s): 17478-622
- 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 September 17, 2012
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
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Warnings
- Do not use this product except under the advice and supervision of a doctor.
- Do not use if bottom ridge of tube cap is exposed
- To avoid contamination, do not touch tip of container to any surface.
- Replace cap after using.
- May cause temporary burning and irritation upon application into the eye.
- Directions
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SODIUM CHLORIDE
sodium chloride ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54868-4698(NDC:17478-622) Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Sodium Chloride (UNII: 451W47IQ8X) (Sodium Cation - UNII:LYR4M0NH37, Chloride Ion - UNII:Q32ZN48698) Sodium Chloride 50 mg in 1 g Inactive Ingredients Ingredient Name Strength Mineral Oil (UNII: T5L8T28FGP) Lanolin (UNII: 7EV65EAW6H) Water (UNII: 059QF0KO0R) Petrolatum (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54868-4698-0 1 in 1 CARTON 1 3.5 g in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part349 03/30/2006 Labeler - Physicians Total Care, Inc. (194123980) Establishment Name Address ID/FEI Business Operations Physicians Total Care, Inc. 194123980 relabel(54868-4698)