Label: EASYSTICK- sodium chlorite liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 81468-0003-1 - Packager: YESUNG GLOBAL.Co.,Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated February 15, 2021
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- 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
EASYSTICK
sodium chlorite liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81468-0003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6) SODIUM CHLORITE 5 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:81468-0003-1 10 g in 1 NOT APPLICABLE; Type 0: Not a Combination Product 01/27/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/27/2021 Labeler - YESUNG GLOBAL.Co.,Ltd (695805936) Registrant - YESUNG GLOBAL.Co.,Ltd (695805936) Establishment Name Address ID/FEI Business Operations YESUNG GLOBAL.Co.,Ltd 695805936 label(81468-0003) Establishment Name Address ID/FEI Business Operations Pure O2 695881145 manufacture(81468-0003)
