NDC 73549-029 Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73549 - Fortress Expert Co., Ltd
- 73549-029 - Hand Sanitizer
Product Packages
NDC Code 73549-029-01
Package Description: 30 mL in 1 BOTTLE
Product Details
What is NDC 73549-029?
What are the uses for Hand Sanitizer?
Which are Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Hand Sanitizer Inactive Ingredients UNII Codes?
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. The UNII codes for the inactive ingredients in this product are:
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- ALOE VERA WHOLE (UNII: KIZ4X2EHYX)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- FRAGRANCE FLORAL ORC0902236 (UNII: R66Z4YW3X0)
- WATER (UNII: 059QF0KO0R)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
What is the NDC to RxNorm Crosswalk for Hand Sanitizer?
- RxCUI: 582753 - ethanol 70 % Topical Solution
- RxCUI: 582753 - ethanol 0.7 ML/ML Topical Solution
- RxCUI: 582753 - ethyl alcohol 70 % Topical Solution
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] 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.
[12] 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".