NDC 78214-001 Sunbeam Wash-free Hand Sanitizer/disinfectant
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 78214 - Xiamen Sunbeam Industries Ltd.
- 78214-001 - Sunbeam Wash-free Hand Sanitizer/disinfectant
Product Packages
NDC Code 78214-001-01
Package Description: 30 mL in 1 BOTTLE
NDC Code 78214-001-02
Package Description: 50 mL in 1 BOTTLE
NDC Code 78214-001-03
Package Description: 60 mL in 1 BOTTLE
NDC Code 78214-001-04
Package Description: 100 mL in 1 BOTTLE
NDC Code 78214-001-05
Package Description: 250 mL in 1 BOTTLE
NDC Code 78214-001-06
Package Description: 350 mL in 1 BOTTLE
NDC Code 78214-001-07
Package Description: 500 mL in 1 BOTTLE
NDC Code 78214-001-08
Package Description: 1000 mL in 1 BOTTLE
NDC Code 78214-001-09
Package Description: 3000 mL in 1 BOTTLE
NDC Code 78214-001-10
Package Description: 5000 mL in 1 BOTTLE
NDC Code 78214-001-11
Package Description: 100000 mL in 1 BOTTLE
NDC Code 78214-001-12
Package Description: 150000 mL in 1 BOTTLE
NDC Code 78214-001-13
Package Description: 220000 mL in 1 BOTTLE
Product Details
What is NDC 78214-001?
What are the uses for Sunbeam Wash-free Hand Sanitizer/disinfectant?
Which are Sunbeam Wash-free Hand Sanitizer/disinfectant UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Sunbeam Wash-free Hand Sanitizer/disinfectant 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:
- TOCOPHEROL (UNII: R0ZB2556P8)
- ALOE (UNII: V5VD430YW9)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- WATER (UNII: 059QF0KO0R)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
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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".