NDC 49825-130 Acne Toner Biolements
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49825 - Bioelements, Inc.
- 49825-130 - Acne Toner
Product Packages
NDC Code 49825-130-02
Package Description: 1 BOTTLE in 1 CARTON / 88 mL in 1 BOTTLE (49825-130-01)
NDC Code 49825-130-04
Package Description: 1 BOTTLE in 1 CARTON / 236 mL in 1 BOTTLE (49825-130-03)
Product Details
What is NDC 49825-130?
What are the uses for Acne Toner Biolements?
Which are Acne Toner Biolements 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 Acne Toner Biolements 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)
- HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- GLYCERIN (UNII: PDC6A3C0OX)
- WINE GRAPE (UNII: 3GOV20705G)
- HONEY (UNII: Y9H1V576FH)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- PINEAPPLE (UNII: 2A88ZO081O)
- LEMON (UNII: 24RS0A988O)
- LIME (CITRUS) (UNII: 8CZS546954)
- LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
- GRAPEFRUIT (UNII: O82C39RR8C)
- ORANGE (UNII: 5EVU04N5QU)
- KIWI FRUIT (UNII: 71ES77LGJC)
- PAPAYA (UNII: KU94FIY6JB)
- GRAPEFRUIT OIL (UNII: YR377U58W9)
- ELEMI (UNII: C13XI009KO)
- ORANGE OIL (UNII: AKN3KSD11B)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- LAVANDIN OIL (UNII: 9RES347CKG)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
What is the NDC to RxNorm Crosswalk for Acne Toner Biolements?
- RxCUI: 248684 - salicylic acid 0.5 % Topical Cream
- RxCUI: 248684 - salicylic acid 5 MG/ML Topical Cream
* 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".