Active Ingredient(S)
Alcohol 65% v/v. Purpose: Antiseptic
Hand Sanitizer
FDA Label NDC 79436-102
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Oingo Products Llc for the product Hand Sanitizer (NDC 79436-102). 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), purpose, use, warnings, do not use, when using this product, stop use and ask a doctor, 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, Hand Sanitizer
Use
for handwashing to decrease bacteria on the skin
Warnings
For external use only, Flammable, keep away from fire or flame, heat, sparks, and sources of static discharge
Do Not Use
- In eyes | on children less than 2 months of age | on open skin wounds
When Using This Product
If in eyes, rinse promptly and thoroughly with water | Discontinue use if irritation and redness develops
Stop Use And Ask A Doctor
If skin irritation or redness occurs or persists for more than 72 hours.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Place enough product on hands to cover all surfaces. Rub hands together until 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)
Inactive Ingredients
water (aqua), propylene glycol,
dimethicone PEG-7 Isostearate, acrylates/ C10-30 Alkyl
Acrylate Crosspolymer, aminomethylpropanediol, tocopherol
acetate, aloe barbadensis leaf juice
Package Label - Principal Display Panel
59 mL NDC: 79436-102-01
* Please review the disclaimer below.
