NDC 76173-1100 The Cellin Sc Bb Cream Spf 25 Pa
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 76173-1100?
What are the uses for The Cellin Sc Bb Cream Spf 25 Pa?
Which are The Cellin Sc Bb Cream Spf 25 Pa UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are The Cellin Sc Bb Cream Spf 25 Pa 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- TALC (UNII: 7SEV7J4R1U)
- HEXYLDECYL MYRISTOYL METHYLAMINOPROPIONATE (UNII: 1959TW0O9A)
- ISOPROPYL ISOSTEARATE (UNII: C67IXB9Y7T)
- NIACINAMIDE (UNII: 25X51I8RD4)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- MAGNESIUM SULFATE (UNII: DE08037SAB)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- PURSLANE (UNII: M6S840WXG5)
- C12-14 PARETH-3 (UNII: 93RY22U87E)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- METHICONE (20 CST) (UNII: 6777U11MKT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- PALMITIC ACID (UNII: 2V16EO95H1)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- ALUMINUM STEARATE (UNII: U6XF9NP8HM)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ADENOSINE (UNII: K72T3FS567)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- BUCKMINSTERFULLERENE (UNII: NP9U26B839)
- ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- CHAMOMILE (UNII: FGL3685T2X)
- SOYBEAN (UNII: L7HT8F1ZOD)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
- PUERARIA MONTANA VAR. LOBATA ROOT (UNII: PET93F4I3C)
- CNIDIUM OFFICINALE ROOT (UNII: 8S3OZD358J)
- PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- XANTHAN GUM (UNII: TTV12P4NEE)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- METHYLINOSITOL (UNII: TF9HZN9T0M)
- PALMITOYL PENTAPEPTIDE-4 (UNII: KK181SM5JG)
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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".