NDC 69740-322 Secura Dimethicone Protectant
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What is NDC 69740-322?
What are the uses for Secura Dimethicone Protectant?
Which are Secura Dimethicone Protectant UNII Codes?
The UNII codes for the active ingredients in this product are:
- MOMETASONE FUROATE (UNII: 04201GDN4R)
- MOMETASONE (UNII: 8HR4QJ6DW8) (Active Moiety)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Secura Dimethicone Protectant 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:
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PROPYLENE GLYCOL STEARATE (UNII: MZM1I680W0)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- WHITE WAX (UNII: 7G1J5DA97F)
- PETROLATUM (UNII: 4T6H12BN9U)
- WATER (UNII: 059QF0KO0R)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PARAFFIN (UNII: I9O0E3H2ZE)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- YELLOW WAX (UNII: 2ZA36H0S2V)
What is the NDC to RxNorm Crosswalk for Secura Dimethicone Protectant?
- RxCUI: 259090 - dimethicone 5 % Topical Cream
- RxCUI: 259090 - dimethicone 50 MG/ML Topical Cream
- RxCUI: 311753 - mometasone furoate 0.1 % Topical Cream
- RxCUI: 311753 - mometasone furoate 1 MG/ML Topical Cream
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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".