NDC | 0363-7500-50 |
Set ID | bda3b9db-5fc4-408c-a5ae-d1eeb3ee308d |
Category | HUMAN OTC DRUG LABEL |
Packager | Walgreen Company |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART349 |
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
-
Warnings
• For use in the eyes only.
• Retain outer carton for full product drug facts.
When using this product
• avoid contamination, do not touch tip of container to any surface.
• replace cap after use.
• this product may cause temporary burning and irritation on being instilled into the eye.
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
WALGREENS SODIUM CHLORIDE OPHTHALMIC 5 PERCENT HYPERTONICITY EYE
sodium chloride ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-7500 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 50 mg in 1 g Inactive Ingredients Ingredient Name Strength LANOLIN ALCOHOLS (UNII: 884C3FA9HE) MINERAL OIL (UNII: T5L8T28FGP) WATER (UNII: 059QF0KO0R) PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-7500-50 1 in 1 CARTON 04/01/2019 1 3.5 g in 1 TUBE; 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 04/01/2019 Labeler - Walgreen Company (008965063)