Label: SUFIYA (hocl- hypochlorous acid liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 82124-701-01, 82124-701-02, 82124-701-03 - Packager: EMSOLUTION Co., Ltd
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated December 29, 2022
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient[s]
- Purpose
- Use[s]
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor
- Keep out of reach of children.
- Directions
- Other information
- Inactive ingredients
- Package Label
-
INGREDIENTS AND APPEARANCE
SUFIYA
hocl(hypochlorous acid) liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82124-701 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID 0.1 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82124-701-01 60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 07/20/2021 2 NDC:82124-701-02 600 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 07/20/2021 3 NDC:82124-701-03 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/20/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/20/2021 Labeler - EMSOLUTION Co., Ltd (694603987) Registrant - EMSOLUTION Co., Ltd (694603987) Establishment Name Address ID/FEI Business Operations EMSOLUTION Co., Ltd 694603987 manufacture(82124-701)