NDC 54973-3403 Young Adult Clearac

Silicon Dioxide, Sulfur, Potassium Dichromate, Activated Charcoal, Calcium Sulfide, Potassium Bromide, Arsenic Trioxide And Potassium Chloride

NDC Product Code 54973-3403

NDC Code: 54973-3403

Proprietary Name: Young Adult Clearac 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: Silicon Dioxide, Sulfur, Potassium Dichromate, Activated Charcoal, Calcium Sulfide, Potassium Bromide, Arsenic Trioxide And Potassium Chloride 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

NDC 54973-3403-1

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

NDC Product Information

Young Adult Clearac with NDC 54973-3403 is a a human over the counter drug product labeled by Hyland's. The generic name of Young Adult Clearac is silicon dioxide, sulfur, potassium dichromate, activated charcoal, calcium sulfide, potassium bromide, arsenic trioxide and potassium chloride. 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 Clearac 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.

  • SILICON DIOXIDE 30 [hp_X]/1
  • SULFUR 30 [hp_X]/1
  • POTASSIUM DICHROMATE 30 [hp_X]/1
  • POTASSIUM BROMIDE 30 [hp_X]/1
  • ARSENIC TRIOXIDE 30 [hp_X]/1
  • POTASSIUM CHLORIDE 9 [hp_X]/1
  • ACTIVATED CHARCOAL 30 [hp_X]/1
  • CALCIUM SULFIDE 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 Clearac Product Label Images

Young Adult Clearac 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

Arsenicum Album 30X HPUSCarbo Vegetabilis 30X HPUSHepar Sulphuris Calcareum 12X HPUSKali Bichromicum 30X HPUSKali Bromatum 30X HPUSKali Muriaticum 9X HPUSSilicea 30X HPUSSulphur 30X HPUS

Purpose

For Acne,Pimples,Blotches,Unhealthy Skin

Uses

Temporarily relieves symptoms associated with acne, including: pimples, blotches or unhealthy skin

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 3 tablets under tongueevery 8 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.