Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Dr. Talbots Tummy Ache Relief NDC 70797-311
Activated charcoal 12 [hp_X]/118mL + 9 more ingredients · Liquid · Oral · Talbot's Pharmaceuticals Family Products, LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70797-311-01 | 7079703110170797031101 | 1 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
- Labeler
- Talbot's Pharmaceuticals Family Products, LLCNDC labeler code 70797
- 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
N470797031101followed by a unit qualifier and the quantityPackage 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.
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.