NDC 11701-046 Baza Protect
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11701 - Coloplast Manufacturing Us, Llc
- 11701-046 - Baza Protect
Product Packages
NDC Code 11701-046-22
Package Description: 4 g in 1 PACKET
NDC Code 11701-046-23
Package Description: 57 g in 1 TUBE
Product Details
What is NDC 11701-046?
What are the uses for Baza Protect?
Which are Baza Protect UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Baza Protect 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:
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- TRICONTANYL POVIDONE (UNII: N0SS3Q238D)
- PETROLATUM (UNII: 4T6H12BN9U)
- LANOLIN (UNII: 7EV65EAW6H)
- PEG-8 STEARATE (UNII: 2P9L47VI5E)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PEG-40 STEARATE (UNII: ECU18C66Q7)
- EDETIC ACID (UNII: 9G34HU7RV0)
- COD LIVER OIL (UNII: BBL281NWFG)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- QUATERNIUM-15 (UNII: E40U03LEM0)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Baza Protect?
- RxCUI: 1053158 - Baza Protect 1 % / 12 % Topical Cream
- RxCUI: 1053158 - dimethicone 10 MG/ML / zinc oxide 120 MG/ML Topical Cream [Baza-Protect]
- RxCUI: 1053158 - Baza Protect (dimethicone 1 % / zinc oxide 12 % ) Topical Cream
- RxCUI: 1053158 - dimethicone 10 MG/ML / ZNO 120 MG/ML Topical Cream [Baza-Protect]
- RxCUI: 637565 - dimethicone 1 % / zinc oxide 12 % Topical Cream
* 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".