NDC 43742-1629 Female Support
Chamomilla,Cimicifuga Racemosa,Helonias Dioica,Mentha Piperita,Senna (cassia - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43742 - Deseret Biologicals, Inc.
- 43742-1629 - Female Support
Product Packages
NDC Code 43742-1629-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43742-1629?
What are the uses for Female Support?
What are Female Support Active Ingredients?
- BLACK COHOSH 3 [hp_X]/mL
- CHAMAELIRIUM LUTEUM ROOT 3 [hp_X]/mL
- CHASTE TREE FRUIT 4 [hp_X]/mL
- CINCHONA OFFICINALIS BARK 8 [hp_X]/mL
- CINNAMON 12 [hp_X]/mL
- CONVALLARIA MAJALIS 8 [hp_X]/mL - A plant genus of the family Asparagaceae that contains CARDIAC GLYCOSIDES.
- CYCLAMEN PURPURASCENS TUBER 8 [hp_X]/mL
- DELPHINIUM STAPHISAGRIA SEED 4 [hp_X]/mL
- GOLDENSEAL 6 [hp_X]/mL
- HEXAPLEX TRUNCULUS HYPOBRANCHIAL GLAND JUICE 12 [hp_X]/mL
- LEDUM PALUSTRE TWIG 4 [hp_X]/mL
- LILIUM LANCIFOLIUM WHOLE FLOWERING 4 [hp_X]/mL
- MATRICARIA RECUTITA 3 [hp_X]/mL
- MENTHA PIPERITA 3 [hp_X]/mL - A plant genus of the family LAMIACEAE that is the source of peppermint oil.
- NAJA NAJA VENOM 15 [hp_X]/mL
- SAFFRON 6 [hp_X]/mL - A plant genus, in the IRIDACEAE family, known as a source of Saffron.
- SENNA LEAF 3 [hp_X]/mL
- VALERIAN 3 [hp_X]/mL - A plant genus of the family VALERIANACEAE, order Dipsacales, subclass Asteridae, class Magnoliopsida. It is best known for the sedative use and valepotriate content of the roots. It is sometimes called Garden Heliotrope but is unrelated to true Heliotrope (HELIOTROPIUM).
- VIOLA ODORATA 3 [hp_X]/mL
Which are Female Support UNII Codes?
The UNII codes for the active ingredients in this product are:
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
- MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ) (Active Moiety)
- BLACK COHOSH (UNII: K73E24S6X9)
- BLACK COHOSH (UNII: K73E24S6X9) (Active Moiety)
- CHAMAELIRIUM LUTEUM ROOT (UNII: DQV54Y5H3U)
- CHAMAELIRIUM LUTEUM ROOT (UNII: DQV54Y5H3U) (Active Moiety)
- MENTHA PIPERITA (UNII: 79M2M2UDA9)
- MENTHA PIPERITA (UNII: 79M2M2UDA9) (Active Moiety)
- SENNA LEAF (UNII: AK7JF626KX)
- SENNA LEAF (UNII: AK7JF626KX) (Active Moiety)
- VALERIAN (UNII: JWF5YAW3QW)
- VALERIAN (UNII: JWF5YAW3QW) (Active Moiety)
- VIOLA ODORATA (UNII: AET12U8B74)
- VIOLA ODORATA (UNII: AET12U8B74) (Active Moiety)
- CHASTE TREE FRUIT (UNII: 433OSF3U8A)
- CHASTE TREE (UNII: 433OSF3U8A) (Active Moiety)
- LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P)
- LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P) (Active Moiety)
- LILIUM LANCIFOLIUM WHOLE FLOWERING (UNII: X67Z2963PI)
- LILIUM LANCIFOLIUM WHOLE FLOWERING (UNII: X67Z2963PI) (Active Moiety)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (Active Moiety)
- SAFFRON (UNII: E849G4X5YJ)
- SAFFRON (UNII: E849G4X5YJ) (Active Moiety)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
- CINCHONA OFFICINALIS BARK (UNII: S003A158SB)
- CINCHONA OFFICINALIS BARK (UNII: S003A158SB) (Active Moiety)
- CONVALLARIA MAJALIS (UNII: QHH4HVF5QE)
- CONVALLARIA MAJALIS (UNII: QHH4HVF5QE) (Active Moiety)
- CYCLAMEN PURPURASCENS TUBER (UNII: G728143D8Q)
- CYCLAMEN PURPURASCENS TUBER (UNII: G728143D8Q) (Active Moiety)
- CINNAMON (UNII: 5S29HWU6QB)
- CINNAMON (UNII: 5S29HWU6QB) (Active Moiety)
- HEXAPLEX TRUNCULUS HYPOBRANCHIAL GLAND JUICE (UNII: IQV54TN60Y)
- HEXAPLEX TRUNCULUS HYPOBRANCHIAL GLAND JUICE (UNII: IQV54TN60Y) (Active Moiety)
- NAJA NAJA VENOM (UNII: ZZ4AG7L7VM)
- NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (Active Moiety)
Which are Female Support 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
Which are the Pharmacologic Classes for Female Support?
* Please review the disclaimer below.
[1] 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.
[2] 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.
[3] 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.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] 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.
[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.
[10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
[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".