NDC 61722-298 Flormar Blur Effect Bb Sunscreen Broad Spectrum Spf 30 03 Dark Medium
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 61722-298?
What are the uses for Flormar Blur Effect Bb Sunscreen Broad Spectrum Spf 30 03 Dark Medium?
Which are Flormar Blur Effect Bb Sunscreen Broad Spectrum Spf 30 03 Dark Medium UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Flormar Blur Effect Bb Sunscreen Broad Spectrum Spf 30 03 Dark Medium 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)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- GLYCERIN (UNII: PDC6A3C0OX)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- LAURETH-12 (UNII: OAH19558U1)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
- PAULLINIA CUPANA SEED (UNII: C21GE7524R)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
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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".