NDC 51439-004 Treatment 101 Acne Clearing Treatment
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51439 - Carepluss Pharma S.a. De C.v.
- 51439-004 - Treatment 101
Product Packages
NDC Code 51439-004-01
Package Description: .06 mg in 1 BOTTLE
Product Details
What is NDC 51439-004?
What are the uses for Treatment 101 Acne Clearing Treatment?
Which are Treatment 101 Acne Clearing Treatment UNII Codes?
The UNII codes for the active ingredients in this product are:
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Treatment 101 Acne Clearing 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)
- CATALINA (UNII: T3JI0587Q7)
- ARNICA MONTANA (UNII: O80TY208ZW)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CETEARETH-12 (UNII: 7V4MR24V5P)
- BROMELAINS (UNII: U182GP2CF3)
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
- MINERAL OIL (UNII: T5L8T28FGP)
- ETHYLENE GLYCOL (UNII: FC72KVT52F)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- TROLAMINE (UNII: 9O3K93S3TK)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- DODECYLBENZENESULFONIC ACID (UNII: 60NSK897G9)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- PIPERINE (UNII: U71XL721QK)
- MINT (UNII: FV98Z8GITP)
- EDETIC ACID (UNII: 9G34HU7RV0)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
What is the NDC to RxNorm Crosswalk for Treatment 101 Acne Clearing Treatment?
- RxCUI: 282727 - sulfur 5 % Topical Solution
- RxCUI: 282727 - sulfur 50 MG/ML Topical Solution
* 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".