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  4. NDC Product Code: 63083-2124 Pms Drops 2124

NDC 63083-2124 Pms Drops 2124

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 63083-2124?
  4. Pms Drops 2124 Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
63083-2124
Proprietary Name:
Pms Drops 2124
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Professional Complementary Health Formulas
Labeler Code:
63083
Product Label ID:
d05bfbbe-d19d-4fd5-8679-bf17d0b61840
Start Marketing Date: [9]
08-15-1984
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 63083-2124-2

Package Description: 59 mL in 1 BOTTLE, DROPPER

Product Details

What is NDC 63083-2124?

The NDC code 63083-2124 is assigned by the FDA to the product Pms Drops 2124 which is product labeled by Professional Complementary Health Formulas. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63083-2124-2 59 ml in 1 bottle, dropper . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Pms Drops 2124?

For the temporary relief of cramping, lower abdominal or back pain, irritability, fatigue, or debility associated with pre-menstrual syndrome.*

Which are Pms Drops 2124 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)
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
  • MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
  • BOS TAURUS PITUITARY GLAND, POSTERIOR (UNII: 7JM57I419K)
  • BOS TAURUS PITUITARY GLAND, POSTERIOR (UNII: 7JM57I419K) (Active Moiety)
  • PULSATILLA MONTANA WHOLE (UNII: 24K790T39B)
  • PULSATILLA MONTANA WHOLE (UNII: 24K790T39B) (Active Moiety)
  • SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2)
  • SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (Active Moiety)
  • SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID)
  • SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (Active Moiety)
  • THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P)
  • THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P) (Active Moiety)
  • VIBURNUM OPULUS BARK (UNII: T1UG6H6805)
  • VIBURNUM OPULUS BARK (UNII: T1UG6H6805) (Active Moiety)
  • LACHESIS MUTA VENOM (UNII: VSW71SS07I)
  • LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
  • ESTROGENS, CONJUGATED (UNII: IU5QR144QX)
  • ESTROGENS, CONJUGATED (UNII: IU5QR144QX) (Active Moiety)
  • PROGESTERONE (UNII: 4G7DS2Q64Y)
  • PROGESTERONE (UNII: 4G7DS2Q64Y) (Active Moiety)

Which are Pms Drops 2124 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:

* Please review the disclaimer below.

Product Footnotes

[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".