NDC 73976-3303 Santotizer Pure I75
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73976 - Santolubes Llc
- 73976-3303 - Santotizer Pure I75
Product Packages
NDC Code 73976-3303-1
Package Description: 3600 mL in 1 PAIL
NDC Code 73976-3303-2
Package Description: 18000 mL in 1 PAIL
NDC Code 73976-3303-3
Package Description: 200000 mL in 1 DRUM
NDC Code 73976-3303-4
Package Description: 1022000 mL in 1 TANK
NDC Code 73976-3303-5
Package Description: 118.294 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 73976-3303?
What are the uses for Santotizer Pure I75?
Which are Santotizer Pure I75 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL ALCOHOL (UNII: ND2M416302) (Active Moiety)
Which are Santotizer Pure I75 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Santotizer Pure I75?
- RxCUI: 1039900 - isopropyl alcohol 75 % Topical Solution
- RxCUI: 1039900 - isopropyl alcohol 0.75 ML/ML Topical Solution
* 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".