Label: D.PRO PACK SOLID- sodium chlorite powder
- NDC Code(s): 75124-0011-1
- Packager: Pure O2
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated April 17, 2021
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- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
D.PRO PACK SOLID
sodium chlorite powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75124-0011 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6) SODIUM CHLORITE 23 g in 100 g Inactive Ingredients Ingredient Name Strength CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM BISULFATE (UNII: BU8V88OWIQ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75124-0011-1 4 g in 1 CONTAINER; Type 0: Not a Combination Product 04/17/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/17/2021 Labeler - Pure O2 (695881145) Registrant - Pure O2 (695881145) Establishment Name Address ID/FEI Business Operations Pure O2 695881145 manufacture(75124-0011)
