NDC 78036-001 Chembrite
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 78036-001-01
Package Description: 200 mL in 1 BOTTLE
NDC Code 78036-001-02
Package Description: 250 mL in 1 BOTTLE
NDC Code 78036-001-03
Package Description: 500 mL in 1 BOTTLE
NDC Code 78036-001-04
Package Description: 1000 mL in 1 BOTTLE
NDC Code 78036-001-05
Package Description: 5000 mL in 1 CONTAINER
NDC Code 78036-001-06
Package Description: 10000 mL in 1 CONTAINER
NDC Code 78036-001-07
Package Description: 20000 mL in 1 CONTAINER
NDC Code 78036-001-08
Package Description: 25000 mL in 1 CONTAINER
NDC Code 78036-001-09
Package Description: 30000 mL in 1 CONTAINER
NDC Code 78036-001-10
Package Description: 200000 mL in 1 CONTAINER
NDC Code 78036-001-11
Package Description: 209000 mL in 1 CONTAINER
NDC Code 78036-001-12
Package Description: 1000000 mL in 1 CONTAINER
Product Details
What is NDC 78036-001?
What are the uses for Chembrite?
Which are Chembrite 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 Chembrite 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)
- CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)
- WATER (UNII: 059QF0KO0R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- TROLAMINE (UNII: 9O3K93S3TK)
- PEG-150 DILAURATE (UNII: CF607I8E19)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
- LEMON OIL, TERPENELESS (UNII: X69W83NI7V)
What is the NDC to RxNorm Crosswalk for Chembrite?
- RxCUI: 2371247 - isopropyl alcohol 60 % Topical Gel
- RxCUI: 2371247 - isopropyl alcohol 0.6 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".