NDC 69299-101 Quick Dry Acne Treatment
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69299 - Dr. Thrower's Skincare, Inc.
- 69299-101 - Quick Dry Acne Treatment
Product Packages
NDC Code 69299-101-51
Package Description: 1 BOTTLE in 1 BOX / 30 mL in 1 BOTTLE (69299-101-11)
Product Details
What is NDC 69299-101?
What are the uses for Quick Dry Acne Treatment?
Which are Quick Dry Acne Treatment UNII Codes?
The UNII codes for the active ingredients in this product are:
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Quick Dry Acne 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:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
- FILIPENDULA ULMARIA WHOLE (UNII: 3LH0M209LN)
- CAMPHOR OIL (UNII: 75IZZ8Y727)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- PEG-8 DIMETHICONE (UNII: GIA7T764OD)
- GLYCERIN (UNII: PDC6A3C0OX)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM PROPOXYHYDROXYPROPYL THIOSULFATE SILICA (UNII: 208G222332)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
What is the NDC to RxNorm Crosswalk for Quick Dry Acne Treatment?
- RxCUI: 240725 - sulfur 10 % Topical Lotion
- RxCUI: 240725 - sulfur 100 MG/ML Topical Lotion
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[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".