NDC 81886-101 Hand Sanitizer Alcohol 75%

NDC Product Information

Hand Sanitizer Alcohol 75% with NDC 81886-101 is product labeled by Frog Prince (fujian) Baby & Child Care Products Co., Ltd.. The product's dosage form is and is administered via form.

RxNorm Crosswalk

What is RxNorm?
RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) (RxCUI) to each NDC.

The RxNorm Crosswalk for this NDC code indicates a single concept unique identifier (RXCUI) is associated with this product:


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.

  • CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
  • ALOE VERA FLOWER (UNII: 575DY8C1ER)
  • AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • 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: Frog Prince (fujian) Baby & Child Care Products Co., Ltd.
Labeler Code: 81886
Start Marketing Date: 05-12-2021 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.

Hand Sanitizer Alcohol 75% 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

Active Ingredient

ALCOHOL 75%

Purpose

ANTISEPTIC

Use

HAND SANITIZER TO HELP REDUCE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE. FOR USE WHEN SOAP AND WATER ARE NOT AVAILABLE.

Warnings

  • FOR EXTERNAL USE ONLY.KEEP AWAY FROM HEAT OR FLAME.DO NOT USEIN CHILDREN LESS THAN 2 MONTHS OF AGEON OPEN SKIN WOUNDSWHEN 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.

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 AT 1-800-222-1222.

Directions

  • PLACE ENOUGH PRODUCT IN YOUR 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

  • STORE BETWEEN 15-30°C (59-86°F)AVOID FREEZING AND EXCESSIVE HEAT ABOVE 40°C (104°F)

Inactive Ingredients

ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, ALOE BARBADENSIS LEAF EXTRACT, AMINOMETHYL PROPANOL, BUTYLENE GLYCOL, GLYCERIN, WATER (AQUA).

* Please review the disclaimer below.