NDC 71727-106 Puripatch For Acne Treatment
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71727 - Imode Korea, Inc.
- 71727-106 - Puripatch For Acne Treatment
Product Packages
NDC Code 71727-106-02
Package Description: 72 PATCH in 1 BOX / 12.25 mm in 1 PATCH (71727-106-01)
Product Details
What is NDC 71727-106?
What are the uses for Puripatch For Acne Treatment?
Which are Puripatch For Acne Treatment 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 Puripatch For 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:
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- KAOLIN (UNII: 24H4NWX5CO)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- LINALOOL, (-)- (UNII: 3U21E3V8I2)
- WATER (UNII: 059QF0KO0R)
- ACRYLIC ACID/DIMETHICONE METHACRYLATE/ETHYLHEXYL ACRYLATE COPOLYMER (UNII: E5024Y9FFQ)
- EPILOBIUM ANGUSTIFOLIUM WHOLE (UNII: C278QS9YBT)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER (UNII: 788QAG3W8A)
- NONOXYNOL-30 (UNII: JJX07DG188)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- VITIS VINIFERA SEED (UNII: C34U15ICXA)
- LAURETH-7 (UNII: Z95S6G8201)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)
- ALCOHOL (UNII: 3K9958V90M)
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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".