Fem Pro Drops Liquid
NDC 63083-2025
View dosage, usage, ingredients, routes, and UNII mappings.
Product Information
Fem Pro Drops is a UNAPPROVED HOMEOPATHIC-approved product labeled by Professional Complementary Health Formulas. This medication is typically used as a estrogen receptor agonists [moa]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 63083-2025 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
63083-2025
Proprietary Name:
Fem Pro Drops 2025
Non-Proprietary Name: [1]
Fem Pro Drops
Substance Name: [2]
Beta-endorphin Human; Black Cohosh; Bos Taurus Pituitary Gland, Posterior; Caulophyllum Thalictroides Root; Chaste Tree Fruit; Estrogens, Conjugated; Progesterone; Rubus Idaeus Fruit Volatile Oil
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:
Clinical Specifications
Dosage Form:
Liquid
- A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.
Labeler & Regulatory Data
Labeler Name: [5]
Labeler Code:
63083
Product Label ID:
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Marketing Timeline
Start Marketing Date: [9]
08-15-1984
Listing Expiration Date: [11]
12-31-2027
Exclude Flag: [12]
N
Code Structure Chart
Product Details
What is NDC 63083-2025?
The NDC code 63083-2025 is assigned by the FDA to the product Fem Pro Drops 2025. This pharmaceutical product is labeled by Professional Complementary Health Formulas and is currently categorized as listed product. The medication is a liquid administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 63083-2025-2. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.
What are the uses of this product?
For the temporary relief of painful or heavy menses, abdominal cramping, or backache.*
What are Active Ingredients of this product?
An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
- BETA-ENDORPHIN HUMAN 30 [hp_X]/59mL
- BLACK COHOSH 6 [hp_X]/59mL
- BOS TAURUS PITUITARY GLAND, POSTERIOR 12 [hp_X]/59mL
- CAULOPHYLLUM THALICTROIDES ROOT 6 [hp_X]/59mL
- CHASTE TREE FRUIT 3 [hp_X]/59mL
- ESTROGENS, CONJUGATED 30 [hp_X]/59mL - A pharmaceutical preparation containing a mixture of water-soluble, conjugated estrogens derived wholly or in part from URINE of pregnant mares or synthetically from ESTRONE and EQUILIN. It contains a sodium-salt mixture of estrone sulfate (52-62%) and equilin sulfate (22-30%) with a total of the two between 80-88%. Other concomitant conjugates include 17-alpha-dihydroequilin, 17-alpha-estradiol, and 17-beta-dihydroequilin. The potency of the preparation is expressed in terms of an equivalent quantity of sodium estrone sulfate.
- PROGESTERONE 30 [hp_X]/59mL - The major progestational steroid that is secreted primarily by the CORPUS LUTEUM and the PLACENTA. Progesterone acts on the UTERUS, the MAMMARY GLANDS and the BRAIN. It is required in EMBRYO IMPLANTATION; PREGNANCY maintenance, and the development of mammary tissue for MILK production. Progesterone, converted from PREGNENOLONE, also serves as an intermediate in the biosynthesis of GONADAL STEROID HORMONES and adrenal CORTICOSTEROIDS.
- RUBUS IDAEUS FRUIT VOLATILE OIL 6 [hp_X]/59mL
Which are the associated 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 the Inactive Ingredients associated 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)
Which are the Pharmacologic Classes of this product?
A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.
* Please review the full disclaimer at the bottom of this page.
Product & Regulatory Definitions
What is the Non-Proprietary Name? The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
What is the Substance Name? An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
What kind of product is this? Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
What is the Marketing Category? Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".
