NDC 61722-160 Flormar Reborn Bb Sunscreen Broad Spectrum Spf 30 Cp01 Rose
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What is NDC 61722-160?
What are the uses for Flormar Reborn Bb Sunscreen Broad Spectrum Spf 30 Cp01 Rose?
Which are Flormar Reborn Bb Sunscreen Broad Spectrum Spf 30 Cp01 Rose UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Flormar Reborn Bb Sunscreen Broad Spectrum Spf 30 Cp01 Rose 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:
- NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- OCTYLDODECYL STEAROYL STEARATE (UNII: 3D47Q6D93C)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- CANDELILLA WAX (UNII: WL0328HX19)
- PENTAERYTHRITYL TETRABEHENATE (UNII: 9MNZ044IRY)
- ISOCETYL STEAROYL STEARATE (UNII: IJV4LS383R)
- JOJOBA OIL (UNII: 724GKU717M)
- SQUALANE (UNII: GW89575KF9)
- NYLON-12 (UNII: 446U8J075B)
- POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- TOCOPHEROL (UNII: R0ZB2556P8)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- BENZYL SALICYLATE (UNII: WAO5MNK9TU)
- GERANIOL (UNII: L837108USY)
- COUMARIN (UNII: A4VZ22K1WT)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
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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".