NDC 69711-370 Lunchboxwax Body Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69711 - Derma Soleil
- 69711-370 - Lunchboxwax Body Spf 30
Product Packages
NDC Code 69711-370-01
Package Description: 100 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 69711-370?
What are the uses for Lunchboxwax Body Spf 30?
Which are Lunchboxwax Body 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)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Lunchboxwax Body 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:
- MAURITIA FLEXUOSA FRUIT OIL (UNII: 48H19MS04L)
- DISODIUM LAURIMINODIPROPIONATE TOCOPHERYL PHOSPHATES (UNII: 0K5Y9U1P6M)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- CALENDULA OFFICINALIS SEED OIL (UNII: 9JS8DS42SV)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- LAURIC ACID (UNII: 1160N9NU9U)
- AMYLOSE, TAPIOCA (UNII: FL6W3SJ5M7)
- BROWN IRON OXIDE (UNII: 1N032N7MFO)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- AMINOPROPYL ASCORBYL PHOSPHATE (UNII: 290O2PQ83R)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- XANTHAN GUM (UNII: TTV12P4NEE)
- EVENING PRIMROSE OIL (UNII: 3Q9L08K71N)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- GLYCERYL ISOSTEARATE (UNII: HYE7O27HAO)
- MICA (UNII: V8A1AW0880)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SODIUM SALICYLATE (UNII: WIQ1H85SYP)
- SORBIC ACID (UNII: X045WJ989B)
- GRAPE SEED OIL (UNII: 930MLC8XGG)
- JOJOBA OIL (UNII: 724GKU717M)
- CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
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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".