NDC 17312-030 Heartburn Relief

Carbo More

NDC Product Code 17312-030

NDC Code: 17312-030

Proprietary Name: Heartburn Relief 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: Carbo More 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: DIAMOND (C48338)
Size(s):
13 MM
Imprint(s):
TRP
Score: 1

Code Structure
  • 17312 - Trp Company
    • 17312-030 - Heartburn Relief

NDC 17312-030-14

Package Description: 1 BOTTLE in 1 PACKAGE > 50 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE

NDC Product Information

Heartburn Relief with NDC 17312-030 is a a human over the counter drug product labeled by Trp Company. The generic name of Heartburn Relief is carbo more. The product's dosage form is tablet, orally disintegrating and is administered via oral form.

Labeler Name: Trp Company

Dosage Form: Tablet, Orally Disintegrating - A solid dosage form containing medicinal substances which disintegrates rapidly, usually within a matter of seconds, when placed upon the tongue.

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.


Heartburn Relief 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.

  • POTASSIUM DICHROMATE 6 [hp_X]/1
  • CHELIDONIUM MAJUS 6 [hp_X]/1
  • SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 6 [hp_X]/1
  • GINGER 6 [hp_X]/1
  • IRIS VERSICOLOR ROOT 6 [hp_X]/1
  • ACTIVATED CHARCOAL 6 [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.

  • MANNITOL (UNII: 3OWL53L36A)
  • SORBITOL (UNII: 506T60A25R)
  • CROSPOVIDONE (UNII: 68401960MK)
  • CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
  • COPOVIDONE (UNII: D9C330MD8B)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • LACTOSE (UNII: J2B2A4N98G)
  • MAGNESIUM STEARATE (UNII: 70097M6I30)

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.

* Please review the disclaimer below.

Heartburn Relief Product Label Images

Heartburn Relief 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

Otc - Purpose

Carbo vegetabilis HPUS - Gas, Sour burping, Bloating

Chelidonium majus HPUS - Pain after food or alcohol intake

Iris versicolor HPUS - Burning sensation

Kali bichromicum HPUS - Chronic sensation of ulcer

Natrum phosphoricum HPUS - Acid (reflux) belching

Zingiber officinale HPUS - Indigestion

Indications & Usage

Uses:*According to homeopathic indications these ingredients temporarily relieve symptoms such as: • indigestion • acid (reflux) belching • sour burping • sensation of ulcer • burning sensation. * These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Warnings

  • Warnings:USE ONLY AFTER DIAGNOSIS BY A PHYSICIAN AND UNDER THE SUPERVISION OF A PHYSICIAN. This product is intended to complement, not replace, standard medical treatment.Initial worsening of symptoms may occur.A physician should always be consulted to rule out serious causes.

  • In case of overdose, get medical help or contact a Poison Control Center right away.Stop use and ask a doctor if:You experience worsening symptoms.If symptoms last longer than 7 days.

Otc - Pregnancy Or Breast Feeding

If pregnant or breast-feeding, ask a health professional before use.

Directions

  • Suitable for adults and children 12 years and above.Dissolve entire tablet under tongue.Do not chew or swallow whole.Take 1 tablet 3 times a day or as directed by a physician.Use up to 6 times a day as needed.Take at least 10 minutes before or at least 10 minutes after eating or drinking.Children under the age of 12: consult a physician before use.Homeopathic remedies may not be effective for everyone.

Other Information

  • There are no known contraindications.Active ingredients are micro-diluted in accordance with the Homeopathic Pharmacopoeia of the United States and are therefore non-toxic with no known side effects.Store in a cool dark location.

Inactive Ingredients

Advantol® 300, Lactose, Magnesium Stearate, Mannitol, Microcrystalline Cellulose.

Otc - Questions

Www.thereliefproducts.com, 1-888-969-6855

Active Ingredients

Active Ingredients

Carbo vegetabilis HPUS 6x, 12x, 18x

Chelidonium majus HPUS 6x, 12x, 18x

Iris versicolor HPUS 6x, 12x, 18x

Kali bichromicum HPUS 6x, 12x, 18x

Natrum phosphoricum HPUS 6x, 12x,18x

Zingiber officinale HPUS 6x, 12x, 18x
"HPUS" indicates the active ingredients are in the Homeopathic Pharmacopoeia of the United States.

* Please review the disclaimer below.

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