Label: CLEANZGUARD HAND SANITIZER- isopropyl alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 79743-130-01, 79743-130-02, 79743-130-04, 79743-130-08, view more79743-130-32 - Packager: Famco Global Llc
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated July 24, 2020
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)
- Drug Facts
- Active Ingredient
- Purpose
- Uses
- DOSAGE & ADMINISTRATION
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WARNINGS
Warnings Flammable, Keep away from Fire or Flame
For External Use Only
Discolors some fabrics. Harmful to wood finishes and plastics.
When using this product Keep out of eyes, ears and mouth. In case of eye contact, flush eyes with water.
Do NOT ingest.
Stop Use and Ask a Doctor if irritation or redness develops and conditions persist.
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
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SPL UNCLASSIFIED SECTION
• Guards Against 99%of Germs & Viruses
• Cleanz Without Water
• Provides Protection
Made in USA
Scent Free
Cleanzguard is based on the Active Ingredient Isopropyl Alcohol in a unique, non drying, moisturizing and conditioning formulation. CleanzGuard guards 99.% of most common germs that may cause illness, in just 15 seconds. No Water Needed.
SDS : www.cleanzguard.com
Emergency Telephone Number
Chemtrec US 1-800-424-9300
International 1+ 703-527-3887
FAMCO GLOBAL PRODUCTS
844-4-CLEANZ
famcoglobal.com
Gardena, California 90248
- Packaging
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INGREDIENTS AND APPEARANCE
CLEANZGUARD HAND SANITIZER
isopropyl alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79743-130 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 75 mL in 100 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) HYDROGEN PEROXIDE (UNII: BBX060AN9V) WATER (UNII: 059QF0KO0R) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79743-130-02 59 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/01/2020 2 NDC:79743-130-04 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/01/2020 3 NDC:79743-130-08 236 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/01/2020 4 NDC:79743-130-32 946 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/01/2020 5 NDC:79743-130-01 3785 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 05/01/2020 Labeler - Famco Global Llc (109831810)