Active Ingredient(S)
Ethyl Alcohol 62.5% v/v…………………..……... Antiseptic
The following Structured Product Label (SPL) was submitted to the FDA by Oingo Products Llc for the product Hand Sanitizer (NDC 79436-101). 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(s), use, warnings, do not use, when using, stop use and ask a doctor, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Ethyl Alcohol 62.5% v/v…………………..……... Antiseptic
Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
For external use only | Flammable, keep away from fire or flame, heat, sparks, and sources of static discharge
In eyes | on children less than 2 months of age | on open skin wounds
If in eyes, rinse promptly and thoroughly with water | Discontinue use if irritation and redness Develops
if skin irritation or redness occurs
or persists for more than 72 hours.
If swallowed, get medical help
or contact a Poison Control Center right away.
Apply product onto hands, spread thoroughly and
rub dry | Supervise children under 6 years of age when using
this product to avoid swallowing.
Other Information For additional information, see Safety Data
Sheets (SDS) | For emergency medical information in USA and
Canada, call 1-888-255-3924 | Store between 15-
30C (59-86F) | Avoid freexing and excessive heat above 40C
(104F)
water (aqua), propylene glycol,
dimethicone PEG-7 Isostearate, acrylates/ C10-30 Alkyl
Acrylate Crosspolymer, aminomethylpropanediol, tocopherol
acetate, aloe barbadensis leaf juice
Antiseptic, Hand Sanitizer
* Please review the disclaimer below.