Label: SALINE- sodium chloride solution/ drops
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Contains inactivated NDC Code(s)
NDC Code(s): 48951-9998-1 - Packager: Uriel Pharmacy Inc
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated February 2, 2010
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- Official Label (Printer Friendly)
- 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