NDC 69711-909 Derma Soleil Kids Natural Sunblock Spf 45
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69711 - Biological Health Group
- 69711-909 - Derma Soleil Kids Natural Sunblock Spf 45
Product Characteristics
Product Packages
NDC Code 69711-909-01
Package Description: 120 mL in 1 BOTTLE
NDC Code 69711-909-02
Package Description: 240 mL in 1 BOTTLE
Product Details
What is NDC 69711-909?
What are the uses for Derma Soleil Kids Natural Sunblock Spf 45?
Which are Derma Soleil Kids Natural Sunblock Spf 45 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Derma Soleil Kids Natural Sunblock Spf 45 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
- CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
- EDETIC ACID (UNII: 9G34HU7RV0)
- EVENING PRIMROSE OIL (UNII: 3Q9L08K71N)
- CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- LEVULINIC ACID (UNII: RYX5QG61EI)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- WATER (UNII: 059QF0KO0R)
- GRAPE SEED OIL (UNII: 930MLC8XGG)
- HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL)
- JOJOBA OIL (UNII: 724GKU717M)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- SODIUM ANISATE (UNII: F9WFJ28MV9)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
* 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".