NDC 60232-7700 Elta Lite Tar
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 60232-7700?
What are the uses for Elta Lite Tar?
Which are Elta Lite Tar UNII Codes?
The UNII codes for the active ingredients in this product are:
- COAL TAR (UNII: R533ESO2EC)
- COAL TAR (UNII: R533ESO2EC) (Active Moiety)
Which are Elta Lite Tar 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)
- PETROLATUM (UNII: 4T6H12BN9U)
- ALCOHOL (UNII: 3K9958V90M)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- DIETHANOLAMINE CETYL PHOSPHATE (UNII: 4UG0316V9S)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- XANTHAN GUM (UNII: TTV12P4NEE)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- PEG-150 STEARATE (UNII: 7BSG7DF10Q)
- STEARETH-20 (UNII: L0Q8IK9E08)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
- TROLAMINE (UNII: 9O3K93S3TK)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ETHYLPARABEN (UNII: 14255EXE39)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
What is the NDC to RxNorm Crosswalk for Elta Lite Tar?
- RxCUI: 1550738 - coal tar 0.8 % Topical Lotion
- RxCUI: 1550738 - coal tar 8 MG/ML Topical Lotion
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[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".