NDC 75109-518 Alcosm Hand Sanitizer Wipes


NDC Product Code 75109-518

NDC 75109-518-01

Package Description: 135 NOT APPLICABLE in 1 PAIL > 330.4 mL in 1 NOT APPLICABLE

NDC Product Information

Alcosm Hand Sanitizer Wipes with NDC 75109-518 is a a human over the counter drug product labeled by Kangna (zhejiang) Medical Supplies Co., Ltd.. The generic name of Alcosm Hand Sanitizer Wipes is alcohol. The product's dosage form is cloth and is administered via topical form.

Labeler Name: Kangna (zhejiang) Medical Supplies Co., Ltd.

Dosage Form: Cloth - A large piece of relatively flat, absorbent material that contains a drug. It is typically used for applying medication or for cleansing.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Alcosm Hand Sanitizer Wipes Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ALCOHOL 70 mL/100mL

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)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: Kangna (zhejiang) Medical Supplies Co., Ltd.
Labeler Code: 75109
FDA Application Number: part333A What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 10-20-2020 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: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Alcosm Hand Sanitizer Wipes Product Label Images

Alcosm Hand Sanitizer Wipes 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

Ethanol Alcohol 70% by volume




For hand sanitizing to decrease bacteria on the skinapply topically to the skin to help prevent cross contaminationnot recommended for repeated usedries in seconds


●Flammable. Keep away from fire or flame. For

external use only.

●Do not use in or contact the eyes.

●Stop use and ask a doctor if skin irritation or rash


Otc - Keep Out Of Reach Of Children

Keep out of reach of childrenIf swallowed, get medical help or call Poison Control Center immediately.


.Open lid, gently pull back resealable label, remove and use wipe

·Reseal back after use to avoid evaporation of alcohol.

other information

.Store at room temperature 15°-30°C(59°-86°F).

.Lot No. Manufacture date and Expiration date can be found

on canister.

Inactive Ingredients

Aloe Barbadensis Leaf Juice,Carbormer,Diazolidinyl Urea,Glycerin,

Methylparaben,Polysorbate 20,Propylene Glycol,Propylparaben,


* Please review the disclaimer below.