NDC 73040-001 Triple Defense Sunscreen Broad Spectrum Spf 40
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73040 - Rothschild Beauty Group Llc
- 73040-001 - Triple Defense Sunscreen Broad Spectrum Spf 40
Product Packages
NDC Code 73040-001-01
Package Description: 1 TUBE in 1 CARTON / 60 mL in 1 TUBE
Product Details
What is NDC 73040-001?
What are the uses for Triple Defense Sunscreen Broad Spectrum Spf 40?
Which are Triple Defense Sunscreen Broad Spectrum Spf 40 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Triple Defense Sunscreen Broad Spectrum Spf 40 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:
- HAEMATOCOCCUS PLUVIALIS (UNII: 31T0FF0472)
- ZINC SULFATE (UNII: 89DS0H96TB)
- TREHALOSE (UNII: B8WCK70T7I)
- WATER (UNII: 059QF0KO0R)
- XYLITOL (UNII: VCQ006KQ1E)
- KARUM SEED OIL (UNII: 62160PU6FJ)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
- GALACTOARABINAN (UNII: SL4SX1O487)
- PROPANEDIOL (UNII: 5965N8W85T)
- PROPANEDIOL DICAPRYLATE (UNII: C577OMC6UH)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MANNITOL (UNII: 3OWL53L36A)
- MATRICARIA CHAMOMILLA WHOLE (UNII: G0R4UBI2ZZ)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- OLETH-10 (UNII: JD797EF70J)
- SODIUM PHOSPHATE (UNII: SE337SVY37)
- SORBITOL (UNII: 506T60A25R)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- ARTEMISIA CAPILLARIS FLOWER (UNII: KG4724BPZG)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- DIATOMACEOUS EARTH (UNII: 2RF6EJ0M85)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ALPHA LIPOIC ACID (UNII: 73Y7P0K73Y)
- CHIA SEED (UNII: NU0OLX06F8)
- DUNALIELLA SALINA (UNII: F4O1DKI9A6)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PHYMATOLITHON CALCAREUM (UNII: 6J1M3WA0ZK)
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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".