NDC 53727-103 Time Machine Bb
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 53727-103?
What are the uses for Time Machine Bb?
Which are Time Machine 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 Time Machine 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- ARBUTIN (UNII: C5INA23HXF)
- BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: 75D21FL1PI)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
- BABASSU OIL (UNII: 8QSB4M5477)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- TALC (UNII: 7SEV7J4R1U)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- CALCIUM STEARATE (UNII: 776XM7047L)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- DIMETHICONE/DIENE DIMETHICONE CROSSPOLYMER (UNII: RSA9I561OK)
- CODONOPSIS LANCEOLATA ROOT (UNII: 3B7455ZMXH)
- PANAX GINSENG ROOT OIL (UNII: P9T4K47OM0)
- SALVIA MILTIORRHIZA ROOT (UNII: 1693AM5SBN)
- SCROPHULARIA BUERGERIANA ROOT (UNII: CYM875P4NW)
- SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
- PALMITOLEIC ACID (UNII: 209B6YPZ4I)
- ROYAL JELLY (UNII: L497I37F0C)
- ADENOSINE (UNII: K72T3FS567)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- 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".