NDC 75531-010 Ozlab Hand Sanitizer

NDC Product Code 75531-010

NDC CODE: 75531-010

Proprietary Name: Ozlab Hand Sanitizer What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

NDC Code Structure

NDC 75531-010-01

Package Description: 100 mL in 1 BOTTLE, PLASTIC

NDC 75531-010-02

Package Description: 250 mL in 1 BOTTLE, PLASTIC

NDC 75531-010-03

Package Description: 500 mL in 1 BOTTLE, PLASTIC

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Ozlab Hand Sanitizer with NDC 75531-010 is a product labeled by Zhejiang Ounuo Cosmetics Co., Ltd.. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1305100.

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.

  • WATER (UNII: 059QF0KO0R)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
  • AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)

Product Labeler Information

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

Labeler Name: Zhejiang Ounuo Cosmetics Co., Ltd.
Labeler Code: 75531
Start Marketing Date: 05-28-2020 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: 12-31-2021 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.

Ozlab Hand Sanitizer Product Label Images

Ozlab Hand Sanitizer 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

Otc - Active Ingredient

Active ingredient  -- Alcohol   75% (w/w)

Otc - Purpose

Purpose - Antiseptic

Otc - Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away.

Indications & Usage

  • To kill germs and bacteria.recommended for repeated use.

Warnings

For external use only: handsFlammable. Keep away from fire or flame.When using this products, keep out of eyes.Stop using and ask a doctor, if irritation or redness develops.

Dosage & Administration

  • Wet hands thoroughly with product andd rub until dry.

Inactive Ingredient

Water (aqua), propylene glycol, Glycerin, acrylates/c10-30 alkyl acrylate crosspolymer, aminomethyl Propanol, aloe barbadensis leaf extract, fragrance (parfum)

* Please review the disclaimer below.