NDC 63083-5017 Ovarian Drops 5017
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-5017 - Ovarian Drops
Product Packages
NDC Code 63083-5017-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-5017?
What are the uses for Ovarian Drops 5017?
Which are Ovarian Drops 5017 UNII Codes?
The UNII codes for the active ingredients in this product are:
- VIBURNUM OPULUS BARK (UNII: T1UG6H6805)
- VIBURNUM OPULUS BARK (UNII: T1UG6H6805) (Active Moiety)
- CHASTE TREE FRUIT (UNII: 433OSF3U8A)
- CHASTE TREE FRUIT (UNII: 433OSF3U8A) (Active Moiety)
- ALETRIS FARINOSA ROOT (UNII: O021JGR97X)
- ALETRIS FARINOSA ROOT (UNII: O021JGR97X) (Active Moiety)
- AMARYLLIS BELLADONNA WHOLE (UNII: 11B89M58UN)
- AMARYLLIS BELLADONNA WHOLE (UNII: 11B89M58UN) (Active Moiety)
- DIOSCOREA VILLOSA TUBER (UNII: IWY3IWX2G8)
- DIOSCOREA VILLOSA TUBER (UNII: IWY3IWX2G8) (Active Moiety)
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- BLACK COHOSH (UNII: K73E24S6X9)
- BLACK COHOSH (UNII: K73E24S6X9) (Active Moiety)
- BOS TAURUS OVARY (UNII: 66LZN1C747)
- BOS TAURUS OVARY (UNII: 66LZN1C747) (Active Moiety)
- PACKERA AUREA WHOLE (UNII: 5WS1632J8W)
- PACKERA AUREA WHOLE (UNII: 5WS1632J8W) (Active Moiety)
- SUS SCROFA UTERUS (UNII: 2595C75F1P)
- SUS SCROFA UTERUS (UNII: 2595C75F1P) (Active Moiety)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
Which are Ovarian Drops 5017 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)
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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".