NDC 53727-101 Always Triple Bb
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53727 - Cosmecca Korea Co., Ltd.
- 53727-101 - Always Triple Bb
Product Packages
NDC Code 53727-101-01
Package Description: 50 g in 1 BOTTLE
Product Details
What is NDC 53727-101?
What are the uses for Always Triple Bb?
Which are Always Triple Bb UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Always Triple Bb 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)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- PROPYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: O4446S9CRA)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- BIS-PEG/PPG-16/16 PEG/PPG-16/16 DIMETHICONE (UNII: 55A74AJ3KB)
- BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: 75D21FL1PI)
- ARBUTIN (UNII: C5INA23HXF)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- TALC (UNII: 7SEV7J4R1U)
- GLYCERIN (UNII: PDC6A3C0OX)
- CAVIAR, UNSPECIFIED (UNII: 020K6HLU0O)
- ROYAL JELLY (UNII: L497I37F0C)
- MALPIGHIA GLABRA FRUIT (UNII: B94O42LA9M)
- CERESIN (UNII: Q1LS2UJO3A)
- ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- DIMETHICONE/DIENE DIMETHICONE CROSSPOLYMER (UNII: RSA9I561OK)
- ADENOSINE (UNII: K72T3FS567)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
* 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".