Label: NA-ZONE- sodium chloride lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 58291-0011-1 - Packager: Snuva, Inc.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated November 23, 2010
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- ACTIVE INGREDIENT
- INACTIVE INGREDIENTS
- PURPOSE
- USE
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS
- WARNINGS
- NA-ZONE LABEL
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INGREDIENTS AND APPEARANCE
NA-ZONE
sodium chloride lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58291-0011 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE .65 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) EDETATE DISODIUM (UNII: 7FLD91C86K) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) SODIUM BICARBONATE (UNII: 8MDF5V39QO) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58291-0011-1 59 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part349 01/01/1989 Labeler - Snuva, Inc. (807310008) Registrant - Snuva, Inc. (807310008) Establishment Name Address ID/FEI Business Operations Snuva, Inc. 807310008 manufacture