NDC 67510-0403 Epielle Exfoliating Scrub Exfoliating Scrub
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67510 - Kareway Product, Inc.
- 67510-0403 - Epielle Exfoliating Scrub
Product Packages
NDC Code 67510-0403-5
Package Description: 141 g in 1 TUBE
Product Details
What is NDC 67510-0403?
What are the uses for Epielle Exfoliating Scrub Exfoliating Scrub?
Which are Epielle Exfoliating Scrub Exfoliating Scrub 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 Epielle Exfoliating Scrub Exfoliating Scrub 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 COCOYL ISETHIONATE (UNII: 518XTE8493)
- GLYCERIN (UNII: PDC6A3C0OX)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- SYNTHETIC WAX (1200 MW) (UNII: Q3Z4BCH099)
- GLYCOL STEARATE (UNII: 0324G66D0E)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- COCAMIDE (UNII: 3YXD33R71G)
- PEG-6 CAPRYLIC/CAPRIC GLYCERIDES (UNII: GO50W2HWO8)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- XANTHAN GUM (UNII: TTV12P4NEE)
- MENTHOL (UNII: L7T10EIP3A)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
What is the NDC to RxNorm Crosswalk for Epielle Exfoliating Scrub Exfoliating Scrub?
- RxCUI: 317152 - salicylic acid 2 % Topical Cream
- RxCUI: 317152 - salicylic acid 20 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".