NDC 67038-106 No Zit Sherlock Acne Correcting
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 67038-106?
What are the uses for No Zit Sherlock Acne Correcting?
Which are No Zit Sherlock Acne Correcting 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 No Zit Sherlock Acne Correcting 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)
- ALCOHOL (UNII: 3K9958V90M)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY)
- HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)
- SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- UREA (UNII: 8W8T17847W)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- FILIPENDULA ULMARIA WHOLE (UNII: 3LH0M209LN)
What is the NDC to RxNorm Crosswalk for No Zit Sherlock Acne Correcting?
- RxCUI: 1300361 - no 'zit' sherlock correcting serum 1 % Topical Gel
- RxCUI: 1300361 - salicylic acid 0.01 MG/MG Topical Gel [No Zit Sherlock]
- RxCUI: 1300361 - No Zit Sherlock 0.01 MG/MG Topical Gel
- RxCUI: 1300361 - No Zit Sherlock 1 % Topical Gel
- RxCUI: 251380 - salicylic acid 1 % Topical Gel
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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".