NDC 62499-535 Sebobalance Purifying Sebo-absorbing Mask
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 62499-535?
What are the uses for Sebobalance Purifying Sebo-absorbing Mask?
Which are Sebobalance Purifying Sebo-absorbing Mask 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 Sebobalance Purifying Sebo-absorbing Mask 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)
- HECTORITE (UNII: 08X4KI73EZ)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- SORBITOL (UNII: 506T60A25R)
- KAOLIN (UNII: 24H4NWX5CO)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- LACTIC ACID (UNII: 33X04XA5AT)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ALMOND OIL (UNII: 66YXD4DKO9)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- SAGE OIL (UNII: U27K0H1H2O)
- LAVANDIN OIL (UNII: 9RES347CKG)
- GALANGAL OIL (UNII: K0951TAR6Z)
- CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ORANGE OIL (UNII: AKN3KSD11B)
- ALLANTOIN (UNII: 344S277G0Z)
- GLYCERIN (UNII: PDC6A3C0OX)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CARBOMER 934 (UNII: Z135WT9208)
- MASOPROCOL (UNII: 7BO8G1BYQU)
- OLEANOLIC ACID (UNII: 6SMK8R7TGJ)
What is the NDC to RxNorm Crosswalk for Sebobalance Purifying Sebo-absorbing Mask?
- RxCUI: 1014639 - salicylic acid 1 % Paste
- RxCUI: 1014639 - salicylic acid 0.01 MG/MG Paste
- RxCUI: 1014642 - Sebobalance 1 % Topical Paste
- RxCUI: 1014642 - salicylic acid 0.01 MG/MG Paste [Sebobalance]
- RxCUI: 1014642 - Sebobalance 0.01 MG/MG Paste
* 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".