NDC 57520-0598 Vestalcare Spot Free Psoriasis
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57520 - Apotheca Company
- 57520-0598 - Vestalcare Spot Free Psoriasis
Product Characteristics
Product Packages
NDC Code 57520-0598-1
Package Description: 60 TABLET in 1 BOTTLE
Product Details
What is NDC 57520-0598?
What are the uses for Vestalcare Spot Free Psoriasis?
Which are Vestalcare Spot Free Psoriasis UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCIUM SILICATE (UNII: S4255P4G5M)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- LITHIUM CARBONATE (UNII: 2BMD2GNA4V)
- LITHIUM CATION (UNII: 8H8Z5UER66) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- SARSAPARILLA ROOT (UNII: M5552F7Y3Q)
- SARSAPARILLA ROOT (UNII: M5552F7Y3Q) (Active Moiety)
- SULFUR IODIDE (UNII: L6L8KA2AA0)
- SULFUR IODIDE (UNII: L6L8KA2AA0) (Active Moiety)
- THYROID (UNII: 0B4FDL9I6P)
- THYROID (UNII: 0B4FDL9I6P) (Active Moiety)
Which are Vestalcare Spot Free Psoriasis 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:
- DEXTROSE (UNII: IY9XDZ35W2)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
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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".