Active Ingredient
Ethyl alcohol 70%
Cabeau Sanitizer To Go
FDA Label NDC 77087-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Cabeau Inc. for the product Cabeau Sanitizer To Go (NDC 77087-001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, do not use, when using this product, stop use and ask a doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
- to reduce bacteria on the skin that could cause disease
- use when soap and water are not available
Warnings
For external use only: hands
Flammable. Keep away from heat and flame.
Do Not Use
- on children less than 2 months of age
- on open skin wounds
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
Stop Use And Ask A Doctor If
- irritation or redness develop
- condition persists for more than 72 hours
Keep Out Of Reach Of Children.
If swallowed, get medical help or call a Poison Control Center right away.
Directions
- wet hands thoroughly with product and rub hands unitl dry
- for children under 6, use only under adult supervision to avoid swallowing
- not for infants
Other Information
- do not store above 105°F
- may discolor some fabrics
Inactive Ingredients
water, glycerin, propylene glycol, carbomer, sodium hydroxide, fragrace
Questions?
Call toll-free: 1-877-962-2232. Mon-Fri 9-5 p.m. PST
Package Labeling: 30Ml
Label (Label)
Package Labeling: 60Ml
Label2 (Label2)
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