NDC 69937-001 Susanne Kaufmann Suncare Body Broad Spectrum Protection Sunscreen Spf 25 Uvb Uva
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69937 - Susanne Kaufmann Kosmetik Gmbh
- 69937-001 - Susanne Kaufmann Suncare Body Broad Spectrum Protection Sunscreen
Product Packages
NDC Code 69937-001-01
Package Description: 1 BOTTLE, PUMP in 1 CARTON / 100 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 69937-001?
What are the uses for Susanne Kaufmann Suncare Body Broad Spectrum Protection Sunscreen Spf 25 Uvb Uva?
Which are Susanne Kaufmann Suncare Body Broad Spectrum Protection Sunscreen Spf 25 Uvb Uva UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- ENSULIZOLE (UNII: 9YQ9DI1W42)
- ENSULIZOLE (UNII: 9YQ9DI1W42) (Active Moiety)
Which are Susanne Kaufmann Suncare Body Broad Spectrum Protection Sunscreen Spf 25 Uvb Uva 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:
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- BROCCOLI SEED OIL (UNII: SY01LVD4G4)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- POLYSILICONE-15 (UNII: F8DRP5BB29)
- EICOSYL POVIDONE (UNII: XQQ9MKE2BJ)
- SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
- ECTOINE (UNII: 7GXZ3858RY)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- SACCHARIDE ISOMERATE (UNII: W8K377W98I)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- CARDIOSPERMUM HALICACABUM WHOLE (UNII: 185RQ97K0V)
- ECHIUM PLANTAGINEUM SEED OIL (UNII: PIB7XBU8XW)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- JOJOBA OIL (UNII: 724GKU717M)
- SQUALANE (UNII: GW89575KF9)
- TOMATO (UNII: Z4KHF2C175)
- XANTHAN GUM (UNII: TTV12P4NEE)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PHYTATE SODIUM (UNII: 88496G1ERL)
- WATER (UNII: 059QF0KO0R)
- CAPRYLYL CAPRYLATE/CAPRATE (UNII: 22MCG4RSMR)
- COCO-CAPRYLATE (UNII: 4828G836N6)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- GLYCERIN (UNII: PDC6A3C0OX)
* 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".