NDC 71994-007 Chem-free Active Defense Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71994 - Van Laere Llc
- 71994-007 - Chem-free Active Defense Spf 30
Product Packages
NDC Code 71994-007-10
Package Description: 1 TUBE in 1 CARTON / 30 mL in 1 TUBE
NDC Code 71994-007-40
Package Description: 1 TUBE in 1 CARTON / 120 mL in 1 TUBE
Product Details
What is NDC 71994-007?
What are the uses for Chem-free Active Defense Spf 30?
Which are Chem-free Active Defense Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Chem-free Active Defense Spf 30 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)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
- ARGAN OIL (UNII: 4V59G5UW9X)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- SQUALANE (UNII: GW89575KF9)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- LEVOMENOL (UNII: 24WE03BX2T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- FARNESOL (UNII: EB41QIU6JL)
* 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".