NDC 54340-400 Dial Acne Control Deep Cleansing Face Wash
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 54340-400?
What are the uses for Dial Acne Control Deep Cleansing Face Wash?
Which are Dial Acne Control Deep Cleansing Face Wash UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Dial Acne Control Deep Cleansing Face Wash 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)
- SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- GLYCERIN (UNII: PDC6A3C0OX)
- ORANGE JUICE (UNII: 5A9KE2L9L3)
- GRAPEFRUIT JUICE (UNII: JQ9EK2H6BG)
- PASSIFLORA EDULIS FRUIT JUICE (UNII: JS28QQ039D)
- COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE (UNII: 205Z54J075)
- ISOSTEARAMIDOPROPYL MORPHOLINE LACTATE (UNII: 082Y3WQI5K)
- POLYQUATERNIUM-10 (30000 MPA.S AT 2%) (UNII: C7RDC8Y4JS)
- PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
- PEG-200 HYDROGENATED GLYCERYL PALMATE (UNII: W161T051Y1)
- EDETATE SODIUM (UNII: MP1J8420LU)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
What is the NDC to RxNorm Crosswalk for Dial Acne Control Deep Cleansing Face Wash?
- RxCUI: 562600 - salicylic acid 2 % Medicated Liquid Soap
- RxCUI: 562600 - salicylic acid 20 MG/ML Medicated Liquid Soap
- RxCUI: 562600 - salicylic acid 2 % Facial Cleanser Toner
- RxCUI: 562600 - salicylic acid 2 % Facial Scrub
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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".