NDC 43742-1342 Pms Relief
Agnus Castus,Cimicifuga Racemosa,Kali Carbonicum,Lycopodium Clavatum,Saccharum - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43742 - Deseret Biologicals, Inc.
- 43742-1342 - Pms Relief
Product Packages
NDC Code 43742-1342-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43742-1342?
What are the uses for Pms Relief?
What are Pms Relief Active Ingredients?
- ANAMIRTA COCCULUS SEED 12 [hp_X]/mL
- ARISTOLOCHIA CLEMATITIS ROOT 9 [hp_X]/mL
- BLACK COHOSH 6 [hp_X]/mL
- CANDIDA ALBICANS 12 [hp_X]/mL - A unicellular budding fungus which is the principal pathogenic species causing CANDIDIASIS (moniliasis).
- CANIS LUPUS FAMILIARIS MILK 12 [hp_X]/mL
- CHASTE TREE FRUIT 6 [hp_X]/mL
- CONIUM MACULATUM FLOWERING TOP 12 [hp_X]/mL
- CYCLAMEN PURPURASCENS TUBER 12 [hp_X]/mL
- ESTRONE 10 [hp_X]/mL - An aromatized C18 steroid with a 3-hydroxyl group and a 17-ketone, a major mammalian estrogen. It is converted from ANDROSTENEDIONE directly, or from TESTOSTERONE via ESTRADIOL. In humans, it is produced primarily by the cyclic ovaries, PLACENTA, and the ADIPOSE TISSUE of men and postmenopausal women.
- GOLD MONOSULFIDE 12 [hp_X]/mL
- LACHESIS MUTA VENOM 12 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE 6 [hp_X]/mL
- MAGNESIUM CARBONATE 12 [hp_X]/mL
- MICRURUS CORALLINUS VENOM 12 [hp_X]/mL
- POTASSIUM CARBONATE 6 [hp_X]/mL
- PULSATILLA PRATENSIS WHOLE 12 [hp_X]/mL
- SUCROSE 6 [hp_X]/mL - A nonreducing disaccharide composed of GLUCOSE and FRUCTOSE linked via their anomeric carbons. It is obtained commercially from SUGARCANE, sugar beet (BETA VULGARIS), and other plants and used extensively as a food and a sweetener.
- SUS SCROFA HYPOTHALAMUS 8 [hp_X]/mL
- THYROID, BOVINE 6 [hp_X]/mL
- TIN 12 [hp_X]/mL - A trace element that is required in bone formation. It has the atomic symbol Sn, atomic number 50, and atomic weight 118.71.
Which are Pms Relief 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)
- BLACK COHOSH (UNII: K73E24S6X9)
- BLACK COHOSH (UNII: K73E24S6X9) (Active Moiety)
- POTASSIUM CARBONATE (UNII: BQN1B9B9HA)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- SUCROSE (UNII: C151H8M554)
- SUCROSE (UNII: C151H8M554) (Active Moiety)
- THYROID, BOVINE (UNII: MN18OTN73W)
- THYROID, BOVINE (UNII: MN18OTN73W) (Active Moiety)
- SUS SCROFA HYPOTHALAMUS (UNII: N6R0856Z79)
- SUS SCROFA HYPOTHALAMUS (UNII: N6R0856Z79) (Active Moiety)
- ARISTOLOCHIA CLEMATITIS ROOT (UNII: ZY0NX0W00D)
- ARISTOLOCHIA CLEMATITIS ROOT (UNII: ZY0NX0W00D) (Active Moiety)
- ESTRONE (UNII: 2DI9HA706A)
- ESTRONE (UNII: 2DI9HA706A) (Active Moiety)
- GOLD MONOSULFIDE (UNII: 03VC3O9F7W)
- GOLD CATION (1+) (UNII: 3D8CUH9F21) (Active Moiety)
- SULFIDE ION (UNII: G15I91XETI) (Active Moiety)
- CANDIDA ALBICANS (UNII: 4D7G21HDBC)
- CANDIDA ALBICANS (UNII: 4D7G21HDBC) (Active Moiety)
- ANAMIRTA COCCULUS SEED (UNII: 810258W28U)
- ANAMIRTA COCCULUS SEED (UNII: 810258W28U) (Active Moiety)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (Active Moiety)
- CYCLAMEN PURPURASCENS TUBER (UNII: G728143D8Q)
- CYCLAMEN PURPURASCENS TUBER (UNII: G728143D8Q) (Active Moiety)
- MICRURUS CORALLINUS VENOM (UNII: V0S6H36980)
- MICRURUS CORALLINUS VENOM (UNII: V0S6H36980) (Active Moiety)
- CANIS LUPUS FAMILIARIS MILK (UNII: G39P120JQT)
- CANIS LUPUS FAMILIARIS MILK (UNII: G39P120JQT) (Active Moiety)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
- MAGNESIUM CARBONATE (UNII: 0E53J927NA)
- ANEMONE PRATENSIS (UNII: 8E272251DI)
- ANEMONE PRATENSIS (UNII: 8E272251DI) (Active Moiety)
- TIN (UNII: 387GMG9FH5)
- TIN (UNII: 387GMG9FH5) (Active Moiety)
Which are Pms Relief 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 Pms Relief?
* 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.
[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".