NDC 59970-169 Vida Mia Hand Sanitizer Aloe Vera (62%)
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59970 - Navarro Discount Pharmacies,llc
- 59970-169 - Vida Mia Hand Sanitizer Aloe Vera
Product Packages
NDC Code 59970-169-16
Package Description: 453 mL in 1 BOTTLE
Product Details
What is NDC 59970-169?
What are the uses for Vida Mia Hand Sanitizer Aloe Vera (62%)?
Which are Vida Mia Hand Sanitizer Aloe Vera (62%) UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Vida Mia Hand Sanitizer Aloe Vera (62%) 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)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- DIISOPROPYLAMINE (UNII: BR9JLI40NO)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- CETYL ACETATE (UNII: 4Q43814HXS)
- ACETYLATED LANOLIN ALCOHOLS (UNII: SNN716810P)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Vida Mia Hand Sanitizer Aloe Vera (62%)?
- RxCUI: 581660 - ethanol 62 % Topical Gel
- RxCUI: 581660 - ethanol 0.62 ML/ML 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".