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  5. NDC Package Code: 43742-1342-1 Pms Relief

NDC Package 43742-1342-1 Pms Relief

Agnus Castus,Cimicifuga Racemosa,Kali Carbonicum,Lycopodium Clavatum,Saccharum - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
43742-1342-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
43742-1342
Proprietary Name:
Pms Relief
Non-Proprietary Name:
Agnus Castus, Cimicifuga Racemosa, Kali Carbonicum, Lycopodium Clavatum, Saccharum Officinale, Thyroidinum (bovine), Hypothalamus Suis, Aristolochia Clematitis, Folliculinum, Aurum Sulphuratum, Candida Albicans, Cocculus Indicus, Conium Maculatum, Cyclamen Europaeum, Elaps Corallinus, Lac Caninum, Lachesis Mutus, Magnesia Carbonica, Pulsatilla (pratensis), Stannum Metallicum
Substance Name:
Anamirta Cocculus Seed; Aristolochia Clematitis Root; Black Cohosh; Candida Albicans; Canis Lupus Familiaris Milk; Chaste Tree Fruit; Conium Maculatum Flowering Top; Cyclamen Purpurascens Tuber; Estrone; Gold Monosulfide; Lachesis Muta Venom; Lycopodium Clavatum Spore; Magnesium Carbonate; Micrurus Corallinus Venom; Potassium Carbonate; Pulsatilla Pratensis Whole; Sucrose; Sus Scrofa Hypothalamus; Thyroid, Bovine; Tin
Usage Information:
For the temporary relief of symptoms related to premenstrual syndrome, such as mood swings, irritability, anger, sadness, weeping, anxiety, acne, bowel congestion, head pain, muscle pain before menses.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration. For the temporary relief of symptoms related to premenstrual syndrome, such as mood swings, irritability, anger, sadness, weeping, anxiety, acne, bowel congestion, head pain, muscle pain before menses.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
11-Digit NDC Billing Format:
43742134201
Product Type:
Human Otc Drug
Labeler Name:
Deseret Biologicals, Inc.
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):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • 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
  • 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
  • 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
  • SUS SCROFA HYPOTHALAMUS 8 [hp_X]/mL
  • THYROID, BOVINE 6 [hp_X]/mL
  • TIN 12 [hp_X]/mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Fungal Proteins - [CS]
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Increased IgG Production - [PE] (Physiologic Effect)
  • Non-Standardized Fungal Allergenic Extract - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    07-10-2018
    Listing Expiration Date:
    12-31-2025
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 43742-1342-1?

    The NDC Packaged Code 43742-1342-1 is assigned to a package of 30 ml in 1 bottle, dropper of Pms Relief, a human over the counter drug labeled by Deseret Biologicals, Inc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 43742-1342 included in the NDC Directory?

    Yes, Pms Relief with product code 43742-1342 is active and included in the NDC Directory. The product was first marketed by Deseret Biologicals, Inc. on July 10, 2018 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 43742-1342-1?

    The 11-digit format is 43742134201. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-143742-1342-15-4-243742-1342-01