NDC 77725-001 Hand Sanitizer
Ethyl Alcohol
NDC Product Code 77725-001
Proprietary Name: 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.
Non-Proprietary Name: Ethyl Alcohol What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
NDC Code Structure
- 77725 - L.e.d. Cosmetics, Inc.
- 77725-001 - Hand Sanitizer
NDC 77725-001-08
Package Description: 236 mL in 1 BOTTLE, PLASTIC
NDC Product Information
Hand Sanitizer with NDC 77725-001 is a a human over the counter drug product labeled by L.e.d. Cosmetics, Inc.. The generic name of Hand Sanitizer is ethyl alcohol. The product's dosage form is liquid and is administered via topical form.
Labeler Name: L.e.d. Cosmetics, Inc.
Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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.
Hand Sanitizer 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.
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)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- D&C RED NO. 34 (UNII: BAN556989E)
- D&C RED NO. 6 BARIUM LAKE (UNII: K4XZD9W99K)
- FERRIC FERROCYANIDE (UNII: TLE294X33A)
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.
Product Labeler Information
What is the Labeler Name?Name of Company corresponding to the labeler code segment of the Product NDC.
Labeler Name: L.e.d. Cosmetics, Inc.
Labeler Code: 77725
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: 05-26-2020 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.
Hand Sanitizer Product Label Images
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
Medicinal Ingredient
Ethyl Alcohol 70%
Purpose
Antiseptic
Non-Medicinal:
Water(Aqua), Carbomer, Glycerin, Propylene Glycol, Tocopheryl Acetate (Vitamin E), Aminomethyl Propanol, Aloe Barbadensis Leaf Juice, Parfum.May Contain:Yellow 5 Lake (CI 19140), Red 34 (CI 15880), Red 6 Lake (CI 15850), Ferric Ferrocyanide (CI 77510).
Directions:
Put a thumbnail size amount in your palm and rub hands briskly until dry.Note:Children under 6 years of age should be supervised during use.
Storage And Handling
Do not store above 105°C. May discolor certain fabrics.
Caution:
Flammable. Keep away from fire or flame. For external use only. Keep out of eyes. In case of eye contact, immediately flush with water. If swallowed, call a physician. Discontinue use if irritation or redness develop. If condition persists for more than 72 hours, consult a physician.
* Please review the disclaimer below.
