NDC 63083-2138 Dysfunctional Bleeding Drops 2138

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
63083-2138
Proprietary Name:
Dysfunctional Bleeding Drops 2138
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
63083
Start Marketing Date: [9]
08-15-1984
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 63083-2138?

The NDC code 63083-2138 is assigned by the FDA to the product Dysfunctional Bleeding Drops 2138 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 63083-2138-2 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 Dysfunctional Bleeding Drops 2138?

For the temporary relief of occasional mild spotting or menstrual irregularity.*

Which are Dysfunctional Bleeding Drops 2138 UNII Codes?

The UNII codes for the active ingredients in this product are:

  • BOS TAURUS HYPOTHALAMUS (UNII: S6G2NLH4Y7)
  • BOS TAURUS HYPOTHALAMUS (UNII: S6G2NLH4Y7) (Active Moiety)
  • BEEF LIVER (UNII: W8N8R55022)
  • BEEF LIVER (UNII: W8N8R55022) (Active Moiety)
  • BOS TAURUS OVARY (UNII: 66LZN1C747)
  • BOS TAURUS OVARY (UNII: 66LZN1C747) (Active Moiety)
  • BOS TAURUS PITUITARY GLAND, POSTERIOR (UNII: 7JM57I419K)
  • BOS TAURUS PITUITARY GLAND, POSTERIOR (UNII: 7JM57I419K) (Active Moiety)
  • BOS TAURUS SPLEEN (UNII: 190Q9MB3U3)
  • BOS TAURUS SPLEEN (UNII: 190Q9MB3U3) (Active Moiety)
  • SUS SCROFA UTERUS (UNII: 2595C75F1P)
  • SUS SCROFA UTERUS (UNII: 2595C75F1P) (Active Moiety)
  • CHASTE TREE FRUIT (UNII: 433OSF3U8A)
  • CHASTE TREE FRUIT (UNII: 433OSF3U8A) (Active Moiety)
  • COFFEA ARABICA SEED, ROASTED (UNII: 9H58JRT35E)
  • COFFEA ARABICA SEED, ROASTED (UNII: 9H58JRT35E) (Active Moiety)
  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
  • GOLDENSEAL (UNII: ZW3Z11D0JV)
  • GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
  • CAPSELLA BURSA-PASTORIS WHOLE (UNII: W0X9457M59)
  • CAPSELLA BURSA-PASTORIS WHOLE (UNII: W0X9457M59) (Active Moiety)
  • CHAMAELIRIUM LUTEUM ROOT (UNII: DQV54Y5H3U)
  • CHAMAELIRIUM LUTEUM ROOT (UNII: DQV54Y5H3U) (Active Moiety)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
  • TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828)
  • TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828) (Active Moiety)
  • VIBURNUM OPULUS BARK (UNII: T1UG6H6805)
  • VIBURNUM OPULUS BARK (UNII: T1UG6H6805) (Active Moiety)
  • APIS MELLIFERA (UNII: 7S82P3R43Z)
  • APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
  • SELENICEREUS GRANDIFLORUS STEM (UNII: 7114SV0MYK)
  • SELENICEREUS GRANDIFLORUS STEM (UNII: 7114SV0MYK) (Active Moiety)
  • COLLINSONIA CANADENSIS ROOT (UNII: O2630F3XDR)
  • COLLINSONIA CANADENSIS ROOT (UNII: O2630F3XDR) (Active Moiety)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
  • VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z)
  • VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z) (Active Moiety)

Which are Dysfunctional Bleeding Drops 2138 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".