NDC 71876-002 Dynamic Broad Spectrum
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71876 - Prescriber's Choice Inc.
- 71876-002 - Dynamic Broad Spectrum
Product Packages
NDC Code 71876-002-50
Package Description: 50 mL in 1 BOTTLE
Product Details
What is NDC 71876-002?
What are the uses for Dynamic Broad Spectrum?
Which are Dynamic Broad Spectrum UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Dynamic Broad Spectrum 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:
- WATER (UNII: 059QF0KO0R)
- OCTYL STEARATE (UNII: 772Y4UFC8B)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- POLYGLYCERYL-3 OLEATE (UNII: XRQ165498B)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
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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".