NDC 70911-114 Clarify Botanical Clarifying Wash
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70911 - Schweiger Dermatology Group
- 70911-114 - Clarify
Product Characteristics
Product Packages
NDC Code 70911-114-12
Package Description: 1 BOTTLE in 1 CARTON / 100 mL in 1 BOTTLE (70911-114-11)
Product Details
What is NDC 70911-114?
What are the uses for Clarify Botanical Clarifying Wash?
Which are Clarify Botanical Clarifying 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 Clarify Botanical Clarifying 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
- SULFUR (UNII: 70FD1KFU70)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
What is the NDC to RxNorm Crosswalk for Clarify Botanical Clarifying 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".