NDC 72889-726 Bansbao Face Mask (anti-wrinkle)
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72889 - Mengfei Li Inc.
- 72889-726 - Bansbao Face Mask (anti-wrinkle)
Product Characteristics
Product Packages
NDC Code 72889-726-97
Package Description: 20 PATCH in 1 BOX / 28 mL in 1 PATCH
Product Details
What is NDC 72889-726?
What are the uses for Bansbao Face Mask (anti-wrinkle)?
Which are Bansbao Face Mask (anti-wrinkle) UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Bansbao Face Mask (anti-wrinkle) 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)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- HYDROXYETHYL ETHYLCELLULOSE (UNII: ZDN57Z154K)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- TROLAMINE (UNII: 9O3K93S3TK)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- HYDROXYETHYL UREA (UNII: MBQ7DDQ7AR)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- FAGRAEA BERTEROANA FLOWER (UNII: 90D40Y3CDG)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- GLYCEROPHOSPHOINOSITOL CHOLINE (UNII: 3W4V4N5240)
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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".