- Purpose
- Dosage & Administration
- OTC-Active Ingredient
- Inactive Ingredient
- Keep out of reach of children
- Do not use section
- Ask doctor section
- Pregnancy or breast feeding section
- Questions section
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
SALINE
sodium chloride solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-9998 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE 1 [hp_X] Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-9998-1 10 in 1 BOX Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/01/2010 Labeler - Uriel Pharmacy Inc (043471163) Establishment Name Address ID/FEI Business Operations Uriel Pharmacy Inc 043471163 manufacture