NDC 69711-371 Lunchboxwax Mineral Broad Spectrum Sunscreen Face Cream Spf30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69711 - Derma Soleil
- 69711-371 - Lunchboxwax Mineral Broad Spectrum Sunscreen Face Cream Spf30
Product Packages
NDC Code 69711-371-01
Package Description: 50 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 69711-371?
What are the uses for Lunchboxwax Mineral Broad Spectrum Sunscreen Face Cream Spf30?
Which are Lunchboxwax Mineral Broad Spectrum Sunscreen Face Cream Spf30 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 Mineral Broad Spectrum Sunscreen Face Cream Spf30 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".