NDC 67038-104 No Zit Sherlock Acnespot Treatment Spot Treatment
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 67038-104?
What are the uses for No Zit Sherlock Acnespot Treatment Spot Treatment?
Which are No Zit Sherlock Acnespot Treatment Spot Treatment 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 Acnespot Treatment Spot Treatment 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)
- HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- LACTIC ACID (UNII: 33X04XA5AT)
- PPG-26-BUTETH-26 (UNII: 2II1K6TZ4P)
- AMMONIA (UNII: 5138Q19F1X)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- XANTHAN GUM (UNII: TTV12P4NEE)
- FARNESOL (UNII: EB41QIU6JL)
- GLYCERIN (UNII: PDC6A3C0OX)
- NIACINAMIDE (UNII: 25X51I8RD4)
- PANTHENOL (UNII: WV9CM0O67Z)
- EDETATE SODIUM (UNII: MP1J8420LU)
- LAMINARIA OCHROLEUCA (UNII: 4R2124HE76)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SORBITOL (UNII: 506T60A25R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)
- ECHINACEA PURPUREA (UNII: QI7G114Y98)
- LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
- CYMBOPOGON SCHOENANTHUS TOP (UNII: 9SJI1LW39W)
- CYMBOPOGON SCHOENANTHUS OIL (UNII: XE7K568ILO)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- EPILOBIUM ANGUSTIFOLIUM FLOWERING TOP (UNII: 08H094218D)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- BETAINE (UNII: 3SCV180C9W)
- SACCHAROMYCES LYSATE (UNII: R85W246Z1C)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- GERANIOL (UNII: L837108USY)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- YUCCA SCHIDIGERA (UNII: 08A0YG3VIC)
- BENZYL BENZOATE (UNII: N863NB338G)
- CITRAL (UNII: T7EU0O9VPP)
- CHINESE CINNAMON (UNII: WS4CQ062KM)
- SANGUISORBA OFFICINALIS ROOT (UNII: 4NYV2HT01X)
- GINGER (UNII: C5529G5JPQ)
- BENZYL SALICYLATE (UNII: WAO5MNK9TU)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- SERINE (UNII: 452VLY9402)
- GLYCINE (UNII: TE7660XO1C)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- GLUTAMIC ACID (UNII: 3KX376GY7L)
- LYSINE (UNII: K3Z4F929H6)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ALANINE (UNII: OF5P57N2ZX)
- ARGININE (UNII: 94ZLA3W45F)
- COUMARIN (UNII: A4VZ22K1WT)
- LEVOMENOL (UNII: 24WE03BX2T)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- THREONINE (UNII: 2ZD004190S)
- PROLINE (UNII: 9DLQ4CIU6V)
- EUGENOL (UNII: 3T8H1794QW)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- COLA ACUMINATA SEED (UNII: 1F8VIW1479)
- APPLE (UNII: B423VGH5S9)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C VIOLET NO. 2 (UNII: 350KA7O6HK)
What is the NDC to RxNorm Crosswalk for No Zit Sherlock Acnespot Treatment Spot Treatment?
- RxCUI: 1300363 - no 'zit' sherlock spot treatment 2 % Topical Gel
- RxCUI: 1300363 - salicylic acid 0.02 MG/MG Topical Gel [No Zit Sherlock]
- RxCUI: 1300363 - No Zit Sherlock 0.02 MG/MG Topical Gel
- RxCUI: 1300363 - No Zit Sherlock 2 % Topical Gel
- RxCUI: 346298 - salicylic acid 2 % Topical Gel
* 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".