Label: 4 HANDS SANITIZER- hand sanitizer solution
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Contains inactivated NDC Code(s)
NDC Code(s): 73951-0001-1 - Packager: 4 Hands Brewing Company, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated April 14, 2020
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
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SPL UNCLASSIFIED SECTION
This is a hand sanitizer manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency.
The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentag
a. Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (80%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Toba
b. Glycerol (1.45% v/v).
c. Hydrogen peroxide (0.125% v/v).
d. Sterile distilled water or boiled cold water.
The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product. - Active Ingredient
- Purpose
- Use
- Warnings
- Do Not Use
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WHEN USING
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
- STOP USE
- Keep Out of Reach of Children
- Dosage & Administration
- Other Information
- Inactive Ingredients
- 1 GAL Healthcare Personnel Ethyl Alcohol Hand Sanitizer
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INGREDIENTS AND APPEARANCE
4 HANDS SANITIZER
hand sanitizer solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73951-0001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 80 mL in 100 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) HYDROGEN PEROXIDE (UNII: BBX060AN9V) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73951-0001-1 3785.41 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/23/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/23/2020 Labeler - 4 Hands Brewing Company, LLC (007369485) Registrant - 4 Hands Brewing Company, LLC (007369485) Establishment Name Address ID/FEI Business Operations 4 Hands Brewing Company, LLC 007369485 manufacture(73951-0001)
