NDC 49358-547 Mdsolarsciences Spf 30 Mineral Tinted
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49358 - Md Solar Sciences
- 49358-547 - Mdsolarsciences
Product Packages
NDC Code 49358-547-01
Package Description: 1 TUBE in 1 CARTON / 48 g in 1 TUBE
Product Details
What is NDC 49358-547?
What are the uses for Mdsolarsciences Spf 30 Mineral Tinted?
Which are Mdsolarsciences Spf 30 Mineral Tinted UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Mdsolarsciences Spf 30 Mineral Tinted 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:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- GLYCERYL ISOSTEARATE (UNII: HYE7O27HAO)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- POLYSILICONE-15 (UNII: F8DRP5BB29)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CRANBERRY (UNII: 0MVO31Q3QS)
- PUNICA GRANATUM ROOT BARK (UNII: CLV24I3T1D)
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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".