NDC 70108-036 Smart Care Hand Sanitizer 33 Oz
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70108 - Ashtel Studios, Inc
- 70108-036 - Smart Care Hand Sanitizer 33 Oz
Product Packages
NDC Code 70108-036-01
Package Description: 1000 mL in 1 BOTTLE
Product Details
What is NDC 70108-036?
What are the uses for Smart Care Hand Sanitizer 33 Oz?
Which are Smart Care Hand Sanitizer 33 Oz UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Smart Care Hand Sanitizer 33 Oz 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)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- GLYCERIN (UNII: PDC6A3C0OX)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Smart Care Hand Sanitizer 33 Oz?
- 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".