Label: ALLVIRUSU- hypochlorous acid liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 80767-201-01 - Packager: StarParks
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated December 27, 2022
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient[s]
- Purpose
- Use[s]
- Warnings
- When using this product
- Ask a doctor
- Keep out of reach of children.
- Directions
- Other information
- Inactive ingredients
- Package Label
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INGREDIENTS AND APPEARANCE
ALLVIRUSU
hypochlorous acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80767-201 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID 0.002 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:80767-201-01 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/12/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/12/2020 Labeler - StarParks (688505276) Registrant - StarParks (688505276) Establishment Name Address ID/FEI Business Operations StarParks 688505276 manufacture(80767-201)