NDC 54973-3409 Young Adult Moon

Magnesium Phosphate, Dibasic Trihydrate, Caulophyllum Thalictroides Root, Matricaria Chamomilla, Viburnum Opulus Bark, Anamirta Cocculus Seed, Anemone Pulsatilla, Black Cohosh, Citrullus Colocynthis Fruit Pulp, Sepia Officinalis Juice And Tribasic Calcium Phosphate

NDC Product Code 54973-3409

NDC Code: 54973-3409

Proprietary Name: Young Adult Moon What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Magnesium Phosphate, Dibasic Trihydrate, Caulophyllum Thalictroides Root, Matricaria Chamomilla, Viburnum Opulus Bark, Anamirta Cocculus Seed, Anemone Pulsatilla, Black Cohosh, Citrullus Colocynthis Fruit Pulp, Sepia Officinalis Juice And Tribasic Calcium Phosphate 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.

Product Characteristics

Color(s):
WHITE (C48325)
Shape: ROUND (C48348)
Size(s):
9 MM
Score: 1

NDC Code Structure

  • 54973 - Hyland's
    • 54973-3409 - Young Adult Moon

NDC 54973-3409-1

Package Description: 1 BOTTLE, PLASTIC in 1 CARTON > 50 TABLET in 1 BOTTLE, PLASTIC

NDC Product Information

Young Adult Moon with NDC 54973-3409 is a a human over the counter drug product labeled by Hyland's. The generic name of Young Adult Moon is magnesium phosphate, dibasic trihydrate, caulophyllum thalictroides root, matricaria chamomilla, viburnum opulus bark, anamirta cocculus seed, anemone pulsatilla, black cohosh, citrullus colocynthis fruit pulp, sepia officinalis juice and tribasic calcium phosphate. The product's dosage form is tablet and is administered via oral form.

Labeler Name: Hyland's

Dosage Form: Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.

Product Type: Human Otc Drug 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.

Young Adult Moon Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • TRIBASIC CALCIUM PHOSPHATE 12 [hp_X]/1
  • CAULOPHYLLUM THALICTROIDES ROOT 12 [hp_X]/1
  • MATRICARIA CHAMOMILLA 12 [hp_X]/1
  • VIBURNUM OPULUS BARK 12 [hp_X]/1
  • BLACK COHOSH 30 [hp_X]/1
  • CITRULLUS COLOCYNTHIS FRUIT PULP 12 [hp_X]/1
  • SEPIA OFFICINALIS JUICE 30 [hp_X]/1
  • ANAMIRTA COCCULUS SEED 30 [hp_X]/1
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 12 [hp_X]/1
  • ANEMONE PULSATILLA 12 [hp_X]/1

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • ACACIA (UNII: 5C5403N26O)
  • ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Hyland's
Labeler Code: 54973
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 06-01-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Young Adult Moon Product Label Images

Young Adult Moon Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients

Calcarea Phosphorica 12X HPUSCaulophyllum Thalictroides 12X HPUSChamomilla 12X HPUSCimicifuga Racemosa 30X HPUSCocculus Indicus 30X HPUSColocynthis 12X HPUSMagnesia Phosphorica 12X HPUSPulsatilla 12X HPUSSepia 30X HPUSViburnum Opulus 12X HPUS"HPUS" indicates that the active ingredients are in the official HomeopathicPharmacopoeia of the United States.

Purpose

Menstrual Cramps, Irritability, Backache

Uses

Temporarily relieves menstrual symptoms of: pain, cramping, backache, irritability

Warnings

As with any drug, ask a doctor before use if pregnant or breast-feeding.

Other

Consult a physician if symptoms persist for more than 7 days or worsen.

In case of emergency, contact a medical professional or Poison Control Center
immediately. Hyland’s may also be contacted for emergency information aboutour products 24 hours a day, 7 days per week at (800) 624-9659.

*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE,NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.

Otc - Keep Out Of Reach Of Children

Keep this and all medications out of the reach of children. In case of accidental
overdose, contact a medical professional or Poison Control Center immediately.

Directions

Adults and children12 years and overDissolve 2 tablets under tongue every 15 minutesfor up to 4 doses, then every 4 hours until relieved.

Other Information

Do not use if imprinted "SEALED FOR YOUR PROTECTION" tamper-evident bottle cap band is broken or missing.

Inactive Ingredients

Acacia Gum, Lactose

* Please review the disclaimer below.

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