NDC 81209-100 Advanced Gel Hand Sanitizer Refreshing Citrus
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 81209 - Bluetrack, Inc.
- 81209-100 - Advanced Gel Hand Sanitizer Refreshing Citrus
Product Packages
NDC Code 81209-100-01
Package Description: 5000 mL in 1 BOTTLE
NDC Code 81209-100-02
Package Description: 1000 mL in 1 BOTTLE, PUMP
NDC Code 81209-100-03
Package Description: 30 mL in 1 BOTTLE, DISPENSING
NDC Code 81209-100-04
Package Description: 30 mL in 1 BOTTLE, DISPENSING
NDC Code 81209-100-05
Package Description: 60 mL in 1 BOTTLE, DISPENSING
NDC Code 81209-100-06
Package Description: 60 mL in 1 BOTTLE, DISPENSING
Product Details
What is NDC 81209-100?
What are the uses for Advanced Gel Hand Sanitizer Refreshing Citrus?
Which are Advanced Gel Hand Sanitizer Refreshing Citrus UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Advanced Gel Hand Sanitizer Refreshing Citrus 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- FRAGRANCE FRESH CITRUS FLORAL ORC1501495 (UNII: OU4GI2R2WB)
- TOCOPHEROL (UNII: R0ZB2556P8)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- D&C RED NO. 30 (UNII: 2S42T2808B)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- GLYCERIN (UNII: PDC6A3C0OX)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Advanced Gel Hand Sanitizer Refreshing Citrus?
- RxCUI: 581660 - ethanol 62 % Topical Gel
- RxCUI: 581660 - ethanol 0.62 ML/ML Topical Gel
* 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".