NDC codes

FDA NDC Directory
Product NDC (as listed)70797-311Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70797-0311Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
70797-311-0170797031101707970311011 BOTTLE in 1 CARTON (70797-311-01) / 118 mL in 1 BOTTLE (70797-311-04)Marketed from Jul 10, 2020

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Dr. Talbots Tummy Ache Relief
Generic name (nonproprietary)
calendula officinalis, carbo vegetabilis, chamomilla, foeniculum vulgare, lycopodium, nux moschata, zingiber officinale, kali muriaticum, magnesia phosphorica, natrum phosphoricum
Active ingredients
Activated charcoal — 12 [hp_X]/118mLNutmeg — 12 [hp_X]/118mLPotassium chloride — 6 [hp_X]/118mLMatricaria chamomilla — 12 [hp_X]/118mLCalendula officinalis flowering top — 12 [hp_X]/118mLSodium phosphate, Dibasic, Heptahydrate — 6 [hp_X]/118mLLycopodium clavatum spore — 30 [hp_X]/118mLGinger — 12 [hp_X]/118mLMagnesium phosphate, Dibasic trihydrate — 12 [hp_X]/118mLFennel seed — 12 [hp_X]/118mL
Dosage form
Liquid
Route
Oral
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Other FDA classes
Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Food Additives (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Potassium Compounds (Chemical structure)Seed Storage Proteins (Chemical structure)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers
Product ID 70797-311_cda11fa8-ab3d-bd89-e053-2a95a90a8c0eSPL ID cda11fa8-ab3d-bd89-e053-2a95a90a8c0eSPL set ID 91c1e0ae-9999-0ae2-e053-2995a90a2d71UNII 2P3VWU3H10, AEE24M3MQ9, 660YQ98I10, G0R4UBI2ZZ, 18E7415PXQ, 70WT22SF4B, C88X29Y479, C5529G5JPQ, HF539G9L3Q, G3QC02NIE6UPC 0370797300011
Pharmacologic class
Calculi Dissolution Agent; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Osmotic Laxative; Potassium Salt

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N470797031101 followed by a unit qualifier and the quantity

Package 70797-0311-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Uses Uses Temporarily relieves infant discomfort caused by gas colic nausea stomach pressure and cramps diarrhea upset stomach nervous tummy indigestion minor stomach pain excessive stomach acid indications

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70797-311

What is NDC 70797-311?
70797-311 is the product NDC for Dr. Talbots Tummy Ache Relief, Activated charcoal 12 [hp_X]/118mL + 9 more ingredients liquid, listed with the FDA by Talbot's Pharmaceuticals Family Products, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Dr. Talbots Tummy Ache Relief (Calendula officinalis, Carbo vegetabilis, Chamomilla, Foeniculum vulgare, Lycopodium, Nux moschata, Zingiber officinale, Kali muriaticum, Magnesia phosphorica, Natrum phosphoricum).
What is the active ingredient?
Activated charcoal, Nutmeg, Potassium chloride, Matricaria chamomilla, Calendula officinalis flowering top, Sodium phosphate, Dibasic, Heptahydrate, Lycopodium clavatum spore, Ginger, Magnesium phosphate, Dibasic trihydrate, Fennel seed.
Who is the labeler?
Talbot's Pharmaceuticals Family Products, LLC, NDC labeler code 70797. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Dr. Talbots Tummy Ache Relief?
None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

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