NDC 78902-104 Hand Sanitizer Plus Aloe Vera
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 78902 - Jocott Brands, Inc.
- 78902-104 - Hand Sanitizer
Product Packages
NDC Code 78902-104-02
Package Description: 59 mL in 1 BOTTLE
NDC Code 78902-104-04
Package Description: 118 mL in 1 BOTTLE
NDC Code 78902-104-06
Package Description: 177 mL in 1 BOTTLE
NDC Code 78902-104-08
Package Description: 236 mL in 1 BOTTLE
NDC Code 78902-104-16
Package Description: 473 mL in 1 BOTTLE
NDC Code 78902-104-24
Package Description: 739 mL in 1 BOTTLE
NDC Code 78902-104-32
Package Description: 946 mL in 1 BOTTLE
Product Details
What is NDC 78902-104?
What are the uses for Hand Sanitizer Plus Aloe Vera?
Which are Hand Sanitizer Plus Aloe Vera 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 Plus Aloe Vera 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:
- WATER (UNII: 059QF0KO0R)
- POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
- GLYCERIN (UNII: PDC6A3C0OX)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)
What is the NDC to RxNorm Crosswalk for Hand Sanitizer Plus Aloe Vera?
- RxCUI: 902574 - ethanol 65 % Topical Gel
- RxCUI: 902574 - ethanol 0.65 ML/ML Topical Gel
- RxCUI: 902574 - ethyl alcohol 65 % 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".