NDC 81741-111 Piperwaihandsanitizerminty

NDC Product Information

Piperwaihandsanitizerminty with NDC 81741-111 is product labeled by Piperwai, Llc. The product's dosage form is and is administered via form.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • ALOE (UNII: V5VD430YW9)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Piperwai, Llc
Labeler Code: 81741
Start Marketing Date: 03-31-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Piperwaihandsanitizerminty Product Label Images

Piperwaihandsanitizerminty Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index


  • This is a hand rub manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Rub Products During the Public Health Emergency (CoViD-19); Guidance for Industry.The hand rub is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (62%, in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.Glycerol.Sterile distilled water or boiled cold water.

Active Ingredient(S)

Alcohol 62%. Purpose: Antiseptic


Antiseptic, Hand Rub


Reduces the amount of bacteria on hands. Recommended for repeated use.


For external use only. Flammable. Keep away from heat or flame

Do Not Use

Aviod contact with eyes.In case of contact, flush thoroughly with water.

Otc - When Using

When using this product aviod contact with eyes. In case of contact, flush thoroughly with water.Stop use and ask a doctor if irritation occurs.

Otc - Stop Use

Stop use and ask a doctor if irritation or rash occurs.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.


Pump onto dry hands as needed coating evenly.Allow to dry without wipingSupervise children under 6 years oldNot recommended for infants.

Other Information

Do not store above 105F

Inactive Ingredients

Water, Glycerin, Aloe Barbadensis Leaf Juice, Carbomer, Rosmarinus Officinalis (Rosemary) Leaf Oil, Mentha Piperita (Peppermint) Oil, Aminomethyl Propanol

* Please review the disclaimer below.