NDC 77249-104 Seal Non Alcohol Based Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 77249 - Atlantic Care Chemicals Private Limited
- 77249-104 - Seal Non Alcohol Based Hand Sanitizer
Product Packages
NDC Code 77249-104-01
Package Description: .1 L in 1 BOTTLE
NDC Code 77249-104-02
Package Description: .2 L in 1 BOTTLE
NDC Code 77249-104-05
Package Description: .5 L in 1 BOTTLE
NDC Code 77249-104-45
Package Description: 5 L in 1 CAN
Product Details
What is NDC 77249-104?
What are the uses for Seal Non Alcohol Based Hand Sanitizer?
Which are Seal Non Alcohol Based Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Seal Non Alcohol Based 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:
- BOROGLYCERIN (UNII: U3LMU4AN21)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- TROLAMINE (UNII: 9O3K93S3TK)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- WATER (UNII: 059QF0KO0R)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
What is the NDC to RxNorm Crosswalk for Seal Non Alcohol Based Hand Sanitizer?
- RxCUI: 2371245 - benzalkonium chloride 0.5 % Topical Gel
- RxCUI: 2371245 - benzalkonium chloride 0.005 MG/MG Topical Gel
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[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".