Label: DECON-I ANTISEPTIC HAND SANITIZER- isopropyl alcohol solution
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Contains inactivated NDC Code(s)
NDC Code(s): 73837-651-16 - Packager: Maverick Abrasives Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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 January 28, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Purpose
- Uses
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Warnings
Flammable, keep away from fire/flame
For external use only
Do not use
- on children less than 2 months of age
- on open skin wounds
When using this product
- do not get into eyes. In case of contact, rinse eyes thoroughly with water
Stop use and ask a doctor if
- irritation and redness develop
- condition persists for more than 72 hours
- Directions
- Other information
- Inactive Ingredients
- Questions?
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NON-STERILE SOLUTION
ESSENTIAL OILS FRAGRANCE
70% ISOPROPYL ALCOHOL
APPLY AND LET DRY
WARNING SEE SIDE PANEL
DESCRIPTION
Renegade Home & Business Decon-I is a non-sterile, antiseptic hand sanitizer. Solutions with an isopropyl alcohol content of 70% are known and proven to be effective in decreasing bacteria. Fresh and citrusy, our Decon hand sanitizer is effective in decontaminating your skin. This skin-softening formula also contains 100% pure, therapeutic-grade essential oils.
MADE IN THE U.S.A
Manufactured by: Maverick Abrasives, 4340 E Miraloma Ave.,
Anaheim, CA 92807For more ingredient information visit:
www.RenegadeProductsUSA.com or call
TF: [800] 276-5474WARNING
Cancer and Reproductive Harm
www.P65Warnings.ca.gov
- Packaging
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INGREDIENTS AND APPEARANCE
DECON-I ANTISEPTIC HAND SANITIZER
isopropyl alcohol solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73837-651 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) TERT-BUTYL ALCOHOL (UNII: MD83SFE959) HYDROGEN PEROXIDE (UNII: BBX060AN9V) EUCALYPTUS OIL (UNII: 2R04ONI662) ORANGE OIL (UNII: AKN3KSD11B) LEMON OIL (UNII: I9GRO824LL) LIME OIL (UNII: UZH29XGA8G) GRAPEFRUIT OIL (UNII: YR377U58W9) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73837-651-16 474 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/06/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/06/2020 Labeler - Maverick Abrasives Corporation (013826867) Establishment Name Address ID/FEI Business Operations Maverick Abrasives Corporation 013826867 manufacture(73837-651)
