NDC 83093-101 Doitu Acne Microcrystalline Invisible Acne Patch
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 83093 - Guangdong Zhizhen Biological Medicine Co., Ltd.
- 83093-101 - Doitu Acne Microcrystalline Invisible Acne Patch
Product Characteristics
Product Packages
NDC Code 83093-101-01
Package Description: 40 mg in 1 PATCH
NDC Code 83093-101-02
Package Description: 40 mg in 1 PATCH
NDC Code 83093-101-03
Package Description: 40 mg in 1 PATCH
Product Details
What is NDC 83093-101?
What are the uses for Doitu Acne Microcrystalline Invisible Acne Patch?
Which are Doitu Acne Microcrystalline Invisible Acne Patch UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALIX ALBA BARK (UNII: 205MXS71H7)
- SALIX ALBA BARK (UNII: 205MXS71H7) (Active Moiety)
- GINGER (UNII: C5529G5JPQ)
- GINGER (UNII: C5529G5JPQ) (Active Moiety)
- LEVOMENOL (UNII: 24WE03BX2T)
- LEVOMENOL (UNII: 24WE03BX2T) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- AESCULUS CHINENSIS WHOLE (UNII: PGU072XJ6U)
- AESCULUS CHINENSIS WHOLE (UNII: PGU072XJ6U) (Active Moiety)
Which are Doitu Acne Microcrystalline Invisible Acne Patch 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:
- CYCLODEXTRINS (UNII: 7E6SK9QDT8)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52)
- PICHIA JADINII (UNII: 8JRL032K80)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
- STYRENE/ISOPRENE/STYRENE BLOCK COPOLYMER (UNII: K7S96QM8DV)
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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".