NDC 77725-001 Hand Sanitizer
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.
Drug Use Information
Drug Use InformationThe drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.
- This product is used as antiseptic
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 product labeled by L.e.d. Cosmetics, Inc.. 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.
- 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)
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
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: 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 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.