NDC 71544-0022 Vitaplus Fore
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71544 - My Corp.,ltd
- 71544-0022 - Vitaplus Fore
Product Packages
NDC Code 71544-0022-1
Package Description: 4000 mL in 1 DRUM
Product Details
What is NDC 71544-0022?
What are the uses for Vitaplus Fore?
Which are Vitaplus Fore UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Vitaplus Fore 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:
- PINUS DENSIFLORA LEAF (UNII: Q1Q9P50WIY)
- INDICAN (UNII: N187WK1Y1J)
- SORBITOL (UNII: 506T60A25R)
- MALTITOL (UNII: D65DG142WK)
- WATER (UNII: 059QF0KO0R)
- FENNEL SEED (UNII: G3QC02NIE6)
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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".