NDC 68479-503 Special Clearing Booster
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68479 - Dermalogica, Inc.
- 68479-503 - Special Clearing Booster
Product Packages
NDC Code 68479-503-00
Package Description: 2 mL in 1 POUCH
NDC Code 68479-503-02
Package Description: 1 BOTTLE in 1 CARTON / 30 mL in 1 BOTTLE
Product Details
What is NDC 68479-503?
What are the uses for Special Clearing Booster?
Which are Special Clearing Booster UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM)
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (Active Moiety)
Which are Special Clearing Booster 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)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- LAVANDULA ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
- TILIA CORDATA FLOWER (UNII: CFN6G1F6YK)
- CENTAUREA CYANUS FLOWER (UNII: QZ239038YC)
- CHAMOMILE (UNII: FGL3685T2X)
- ST. JOHN'S WORT (UNII: UFH8805FKA)
- NASTURTIUM OFFICINALE FLOWERING TOP (UNII: W1N2U8I64G)
- ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)
- SAGE (UNII: 065C5D077J)
- LEMON (UNII: 24RS0A988O)
- HEDERA HELIX LEAF (UNII: ZP9XFG71A7)
- SAPONARIA OFFICINALIS LEAF (UNII: 3988313MM7)
- TEA TREE OIL (UNII: VIF565UC2G)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ZINC SULFATE (UNII: 89DS0H96TB)
- SULISOBENZONE (UNII: 1W6L629B4K)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
What is the NDC to RxNorm Crosswalk for Special Clearing Booster?
- RxCUI: 1488689 - benzoyl peroxide 5 % Topical Solution
- RxCUI: 1488689 - benzoyl peroxide 50 MG/ML Topical Solution
* Please review the disclaimer below.
[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".