NDC 61924-189 Dermasarra
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61924 - Dermarite Industries, Llc
- 61924-189 - Dermasarra
Product Characteristics
Product Packages
NDC Code 61924-189-08
Package Description: 222 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 61924-189?
What are the uses for Dermasarra?
Which are Dermasarra UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
Which are Dermasarra 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:
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- IMIDUREA (UNII: M629807ATL)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCOL STEARATE (UNII: 0324G66D0E)
- PEG-40 CASTOR OIL (UNII: 4ERD2076EF)
- PEG-4 DILAURATE (UNII: KCR71CW036)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- MINERAL OIL (UNII: T5L8T28FGP)
- PETROLATUM (UNII: 4T6H12BN9U)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM CETOSTEARYL SULFATE (UNII: 7ZBS06BH4B)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
- MENTHOL (UNII: L7T10EIP3A)
What is the NDC to RxNorm Crosswalk for Dermasarra?
- RxCUI: 2059052 - camphor 0.5 % Topical Lotion
- RxCUI: 2059052 - camphor 5 MG/ML Topical Lotion
* 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".