FDA Label for Hand Sanitizer
View Indications, Usage & Precautions
Hand Sanitizer Product Label
The following document was submitted to the FDA by the labeler of this product Oingo Products Llc. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredient(S)
Ethyl Alcohol 62.5% v/v…………………..……... Antiseptic
Use
Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
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
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
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
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
Purpose
Antiseptic, Hand Sanitizer
Package Label - Principal Display Panel
236.5 mL NDC: 79436-101-03
473 mL NDC: 79436-101-04
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