Label: DAILY DOCTOR STERILIZATION PLUS- sodium hypochlorite spray
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Contains inactivated NDC Code(s)
NDC Code(s): 76836-001-01, 76836-001-02 - Packager: GFC Life Science Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated May 1, 2020
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- Active ingredient
- Purpose
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- Warnings
- Directions
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DAILY DOCTOR STERILIZATION PLUS
sodium hypochlorite sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76836-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM HYPOCHLORITE (UNII: DY38VHM5OD) (HYPOCHLORITE ION - UNII:T5UM7HB19N) SODIUM HYPOCHLORITE 0.002 g in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) HYDROCHLORIC ACID (UNII: QTT17582CB) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76836-001-01 60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 04/29/2020 2 NDC:76836-001-02 500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 04/29/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/29/2020 Labeler - GFC Life Science Co., Ltd. (688325518) Registrant - GFC Life Science Co., Ltd. (688325518) Establishment Name Address ID/FEI Business Operations GFC Life Science Co., Ltd. 688325518 manufacture(76836-001)