Label: BT100S- sodium chlorite, citric cid powder
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Contains inactivated NDC Code(s)
NDC Code(s): 77130-0003-1 - Packager: Sejin E&P Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated February 17, 2022
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- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
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- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BT100S
sodium chlorite, citric cid powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77130-0003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) ANHYDROUS CITRIC ACID 0.06 g in 100 g SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6) SODIUM CHLORITE 0.05 g in 100 g Inactive Ingredients Ingredient Name Strength MAGNESIUM SILICATE (UNII: 9B9691B2N9) ALUMINUM SILICATE (UNII: T1FAD4SS2M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:77130-0003-1 40 g in 1 PACKAGE; Type 0: Not a Combination Product 05/02/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/02/2020 Labeler - Sejin E&P Co., Ltd. (694459360) Registrant - Sejin E&P Co., Ltd. (694459360) Establishment Name Address ID/FEI Business Operations Sejin E&P Co., Ltd. 694459360 manufacture(77130-0003)