Label: CABEAU SANITIZER TO GO- alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 77087-001-01, 77087-001-02 - Packager: Cabeau Inc.
- 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 May 6, 2020
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
- Uses
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Warnings
For external use only: hands
Flammable. Keep away from heat and flame.
When using this product
- keep out of eyes. In case of contact with eyes, flush thoroughly with water.
- avoid contact with broken skin
- do not inhale or ingest
- Directions
- Other information
- Inactive ingredients
- Questions?
- Package Labeling: 30ml
- Package Labeling: 60ml
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INGREDIENTS AND APPEARANCE
CABEAU SANITIZER TO GO
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77087-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.7 mL in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:77087-001-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/01/2020 2 NDC:77087-001-02 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 06/01/2020 Labeler - Cabeau Inc. (033683257)