Label: OXICLEANSE- hypochlorous acid, silver spray
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Contains inactivated NDC Code(s)
NDC Code(s): 72136-008-01 - Packager: Oxigenesis, Inc.
- 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 March 1, 2021
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
- KEEP OUT OF REACH OF CHILDREN
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Directions
Pump spray trigger to build pressure and hold. Spray surfaces until lightly misted and allow to air dry.
To refill: use only OxiCleanse™ refill solution.Other information
Do not adulterate or dilute content.
24 Hour Emergency Contact Number: (888) 839-1110
DO NOT USE IF TAMPER PROOF SEAL IS BROKEN OR MISSING.
- Inactive ingredients
- Product label
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INGREDIENTS AND APPEARANCE
OXICLEANSE
hypochlorous acid, silver sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72136-008 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID 50 [ppm] in 1 mL SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER 8 [ppm] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72136-008-01 118.3 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 02/19/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 02/19/2021 Labeler - Oxigenesis, Inc. (006774725) Establishment Name Address ID/FEI Business Operations Oxigenesis, Inc. 006774725 manufacture(72136-008)
