NDC 10802-8081 Derma Cidol 2000
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 10802-8081?
What are the uses for Derma Cidol 2000?
Which are Derma Cidol 2000 UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLOROXYLENOL (UNII: 0F32U78V2Q)
- CHLOROXYLENOL (UNII: 0F32U78V2Q) (Active Moiety)
Which are Derma Cidol 2000 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:
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- POLYETHYLENE GLYCOL 7000 (UNII: Q0JET65GEL)
- PENTAERYTHRITYL TETRASTEARATE (UNII: W9Q3DZS0EG)
- PEG-6 CAPRYLIC/CAPRIC GLYCERIDES (UNII: GO50W2HWO8)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
- SODIUM LAURYL SULFOACETATE (UNII: D0Y70F2B9J)
What is the NDC to RxNorm Crosswalk for Derma Cidol 2000?
- RxCUI: 1603866 - DERMA CIDOL 2000 0.5 % Medicated Liquid Soap
- RxCUI: 1603866 - chloroxylenol 5 MG/ML Medicated Liquid Soap [Derma Cidol]
- RxCUI: 1603866 - Derma Cidol 0.5 % Medicated Liquid Soap
- RxCUI: 1603866 - Derma Cidol 5 MG/ML Medicated Liquid Soap
- RxCUI: 436367 - chloroxylenol 0.5 % Medicated Liquid Soap
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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".