Active Ingredient - Otc - Active Ingredient Section
Ethyl Alcohol 70% (w/w)
The following Structured Product Label (SPL) was submitted to the FDA by Renopac, S.a. De C.v. for the product Sanikit (NDC 79067-004). 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 - otc - active ingredient section, purpose - otc - purpose section, uses - indications and usage section, warnings - warnings sections, when using this product - when using section, stop use and ask a doctor - stop use section, keep out of reach of children - keep out of reach of children section, directions - dosage and administration section, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Ethyl Alcohol 70% (w/w)
Antiseptic
Health care personal hand rub to help reduce bacteria that potentially can cause disease
For external use only.
Flammable.
Kepp away from heat or flame.
Keep out of eyes, ears, and mouth.
In case of contact with eyes, rinse eyes thoroughly with water.
If irritation or rash occur. These may be signs of a serious condition.
If swallowed, get medical help por contact a Poison Control right away.
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.
Store between 15-30°C (59-86°F)
Avoid freezing and excessive heat above 40°C (104°F)
Purified water, carbomer, glycerin, triethanolamine.
SANIKIT 5g NDC - 79067-004-01
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