NDC 69740-342 Secura Starter Kit
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What is NDC 69740-342?
What are the uses for Secura Starter Kit?
Which are Secura Starter Kit UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZETHONIUM CHLORIDE (UNII: PH41D05744)
- BENZETHONIUM (UNII: 1VU15B70BP) (Active Moiety)
- PETROLATUM (UNII: 4T6H12BN9U)
- PETROLATUM (UNII: 4T6H12BN9U) (Active Moiety)
Which are Secura Starter Kit 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:
- ALOE VERA FLOWER (UNII: 575DY8C1ER)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- WATER (UNII: 059QF0KO0R)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- CLOVE OIL (UNII: 578389D6D0)
- D&C GREEN NO. 6 (UNII: 4QP5U84YF7)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- CORN OIL (UNII: 8470G57WFM)
What is the NDC to RxNorm Crosswalk for Secura Starter Kit?
- RxCUI: 1039026 - benzethonium chloride 0.13 % Medicated Liquid Soap
- RxCUI: 1039026 - benzethonium chloride 1.3 MG/ML Medicated Liquid Soap
- RxCUI: 1045424 - {1 (236 ML) (benzethonium chloride 1.3 MG/ML Medicated Liquid Soap) / 1 (72000 MG) (petrolatum 0.988 MG/MG Topical Ointment) } Pack
- RxCUI: 1045424 - benzethonium Cl 0.13 % Medicated Liquid Soap (236 ML) / petrolatum 98.8 % Topical Ointment (72 GM) Pack
- RxCUI: 1045424 - {1 (236 ML benzethonium chloride 0.13 % Medicated Liquid Soap) / 1 (72000 MG petrolatum 98.78 % Topical Ointment) } Pack
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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".