NDC 62499-384 Sebobalance Spot Control
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62499 - Laboratoire Dr. Renaud
- 62499-384 - Sebobalance Spot Control
Product Packages
NDC Code 62499-384-11
Package Description: 1 BOTTLE, WITH APPLICATOR in 1 CARTON / 8 g in 1 BOTTLE, WITH APPLICATOR (62499-384-07)
Product Details
What is NDC 62499-384?
What are the uses for Sebobalance Spot Control?
Which are Sebobalance Spot Control 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 Spot Control 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)
- SORBITOL (UNII: 506T60A25R)
- METHYL GLUCETH-20 (UNII: J3QD0LD11P)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- AMYLOPECTIN (UNII: 4XO4QFV777)
- XANTHAN GUM (UNII: TTV12P4NEE)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
- ARGININE (UNII: 94ZLA3W45F)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- ALLANTOIN (UNII: 344S277G0Z)
- PEUMUS BOLDUS LEAF (UNII: Q4EWM09M3O)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ASCOPHYLLUM NODOSUM (UNII: 168S4EO8YJ)
- CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
- CHAMOMILE (UNII: FGL3685T2X)
- CENTAUREA CYANUS FLOWER (UNII: QZ239038YC)
- TILIA CORDATA FLOWER (UNII: CFN6G1F6YK)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- ASPARAGOPSIS ARMATA (UNII: 2936KN6I1G)
What is the NDC to RxNorm Crosswalk for Sebobalance Spot Control?
- RxCUI: 1020053 - SeboBalance Spot Control 1 % Topical Gel
- RxCUI: 1020053 - salicylic acid 0.01 MG/MG Topical Gel [Sebobalance]
- RxCUI: 1020053 - Sebobalance 0.01 MG/MG Topical Gel
- RxCUI: 1020053 - Sebobalance Spot Control 1 % Topical Gel
- RxCUI: 251380 - salicylic acid 1 % 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".