NDC 68093-6661 Yeast Gard Advanced Treats And Prevents Symptoms Of Vaginal Yeast Infections
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68093 - Wisconsin Pharmacal Company
- 68093-6661 - Yeast Gard Advanced
Product Characteristics
Product Packages
NDC Code 68093-6661-1
Package Description: 1 BOTTLE in 1 CARTON / 60 CAPSULE in 1 BOTTLE
Product Details
What is NDC 68093-6661?
What are the uses for Yeast Gard Advanced Treats And Prevents Symptoms Of Vaginal Yeast Infections?
Which are Yeast Gard Advanced Treats And Prevents Symptoms Of Vaginal Yeast Infections UNII Codes?
The UNII codes for the active ingredients in this product are:
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- COLLINSONIA CANADENSIS ROOT (UNII: O2630F3XDR)
- COLLINSONIA CANADENSIS ROOT (UNII: O2630F3XDR) (Active Moiety)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
Which are Yeast Gard Advanced Treats And Prevents Symptoms Of Vaginal Yeast Infections 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:
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- BROWN RICE (UNII: 659G217HPG)
- BACILLUS COAGULANS (UNII: ISK1LOY57E)
- GELATIN (UNII: 2G86QN327L)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
* Please review the disclaimer below.
[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".