NDC 80026-007 Pumpkin Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 80026 - Reaction Retail, Llc
- 80026-007 - Pumpkin Hand Sanitizer
Product Packages
NDC Code 80026-007-30
Package Description: 30 mL in 1 BOTTLE
NDC Code 80026-007-35
Package Description: 35 mL in 1 BOTTLE
Product Details
What is NDC 80026-007?
What are the uses for Pumpkin Hand Sanitizer?
Which are Pumpkin Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Pumpkin Hand Sanitizer 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- TROLAMINE (UNII: 9O3K93S3TK)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SUCROSE (UNII: C151H8M554)
- CORN (UNII: 0N8672707O)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- BENZYL BENZOATE (UNII: N863NB338G)
- EUGENOL (UNII: 3T8H1794QW)
- COUMARIN (UNII: A4VZ22K1WT)
- CINNAMYL ALCOHOL (UNII: SS8YOP444F)
- .ALPHA.-AMYLCINNAMALDEHYDE (UNII: WC51CA3418)
- CINNAMALDEHYDE (UNII: SR60A3XG0F)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- D&C BLACK NO. 2 (UNII: 4XYU5U00C4)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
What is the NDC to RxNorm Crosswalk for Pumpkin Hand Sanitizer?
- RxCUI: 1305100 - ethanol 75 % Topical Gel
- RxCUI: 1305100 - ethanol 0.75 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".