NDC 63083-2025 Fem Pro Drops 2025
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 63083-2025?
What are the uses for Fem Pro Drops 2025?
Which are Fem Pro Drops 2025 UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHASTE TREE FRUIT (UNII: 433OSF3U8A)
- CHASTE TREE FRUIT (UNII: 433OSF3U8A) (Active Moiety)
- CAULOPHYLLUM THALICTROIDES ROOT (UNII: JTJ6HH6YEH)
- CAULOPHYLLUM THALICTROIDES ROOT (UNII: JTJ6HH6YEH) (Active Moiety)
- BLACK COHOSH (UNII: K73E24S6X9)
- BLACK COHOSH (UNII: K73E24S6X9) (Active Moiety)
- RUBUS IDAEUS FRUIT VOLATILE OIL (UNII: 276X2YNL0K)
- RUBUS IDAEUS FRUIT VOLATILE OIL (UNII: 276X2YNL0K) (Active Moiety)
- BOS TAURUS PITUITARY GLAND, POSTERIOR (UNII: 7JM57I419K)
- BOS TAURUS PITUITARY GLAND, POSTERIOR (UNII: 7JM57I419K) (Active Moiety)
- BETA-ENDORPHIN HUMAN (UNII: 3S51P4W3XQ)
- BETA-ENDORPHIN HUMAN (UNII: 3S51P4W3XQ) (Active Moiety)
- ESTROGENS, CONJUGATED (UNII: IU5QR144QX)
- ESTROGENS, CONJUGATED (UNII: IU5QR144QX) (Active Moiety)
- PROGESTERONE (UNII: 4G7DS2Q64Y)
- PROGESTERONE (UNII: 4G7DS2Q64Y) (Active Moiety)
Which are Fem Pro Drops 2025 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
* 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".