NDC 67996-938 Sani-soft
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 67996-938-01
Package Description: 1200 mL in 1 CARTRIDGE
NDC Code 67996-938-03
Package Description: 350 mL in 1 CARTRIDGE
NDC Code 67996-938-05
Package Description: 540 mL in 1 BOTTLE, PLASTIC
NDC Code 67996-938-06
Package Description: 1 BAG in 1 BOX / 800 mL in 1 BAG
NDC Code 67996-938-07
Package Description: 700 mL in 1 BAG
NDC Code 67996-938-08
Package Description: 1 BAG in 1 BOX / 1000 mL in 1 BAG
NDC Code 67996-938-09
Package Description: 2000 mL in 1 CARTRIDGE
NDC Code 67996-938-10
Package Description: 1000 mL in 1 CARTRIDGE
NDC Code 67996-938-11
Package Description: 1000 mL in 1 BOTTLE, PLASTIC
NDC Code 67996-938-12
Package Description: 1000 mL in 1 BAG
NDC Code 67996-938-13
Package Description: 800 mL in 1 BAG
NDC Code 67996-938-14
Package Description: 3785 mL in 1 BOTTLE, PLASTIC
NDC Code 67996-938-15
Package Description: 946 mL in 1 BOTTLE, PLASTIC
NDC Code 67996-938-17
Package Description: 532 mL in 1 BOTTLE, PLASTIC
NDC Code 67996-938-24
Package Description: 118 mL in 1 BOTTLE, PLASTIC
NDC Code 67996-938-27
Package Description: 800 mL in 1 CARTRIDGE
NDC Code 67996-938-28
Package Description: 149 mL in 1 BOTTLE, PLASTIC
NDC Code 67996-938-55
Package Description: 208200 mL in 1 DRUM
Product Details
What is NDC 67996-938?
What are the uses for Sani-soft?
Which are Sani-soft UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Sani-soft 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 934 (UNII: Z135WT9208)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- DIISOPROPYLAMINE (UNII: BR9JLI40NO)
- CETEARYL ISONONANOATE (UNII: P5O01U99NI)
- CETEARETH-12 (UNII: 7V4MR24V5P)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
* 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".