Label: CLOH LIVING HAND SANITIZER- hypochlorous acid spray
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Contains inactivated NDC Code(s)
NDC Code(s): 79617-100-01, 79617-100-02, 79617-100-03, 79617-100-04, view more79617-100-05 - Packager: SpaceLink Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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 July 20, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- Do not use
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WHEN USING
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. - STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
CLOH LIVING HAND SANITIZER
hypochlorous acid sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79617-100 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID 0.0035 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79617-100-01 500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 07/13/2020 2 NDC:79617-100-02 60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 07/13/2020 3 NDC:79617-100-03 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/13/2020 4 NDC:79617-100-04 4000 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/13/2020 5 NDC:79617-100-05 20000 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/13/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/13/2020 Labeler - SpaceLink Corporation (689464352) Registrant - SpaceLink Corporation (689464352) Establishment Name Address ID/FEI Business Operations SpaceLink Corporation 689464352 manufacture(79617-100)