Dr. Talbots Pain Inflammation Relief NDC 70797-316

NDC codes

FDA NDC Directory

Product NDC (as listed)70797-316Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70797-0316Add 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 NDC	11-digit (billing)	Package	Copy
70797-316-01	70797031601	1 BOTTLE in 1 CARTON (70797-316-01) / 118 mL in 1 BOTTLE (70797-316-04)Marketed from Jul 20, 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 Pain Inflammation Relief
Generic name (nonproprietary): arnica, bellis perennis, calendula officinalis, chamomilla, coffea cruda, hypericum, millefolium, ferrum phosphoricum, kali muriaticum, magnesia phosphorica
Active ingredients: Arabica coffee bean — 12 [hp_X]/118mLMagnesium phosphate, Dibasic — 6 [hp_X]/118mLAchillea millefolium — 12 [hp_X]/118mLArnica montana — 12 [hp_X]/118mLFerrosoferric phosphate — 12 [hp_X]/118mLHypericum perforatum — 12 [hp_X]/118mLBellis perennis — 12 [hp_X]/118mLCalendula officinalis flowering top — 12 [hp_X]/118mLMatricaria chamomilla — 12 [hp_X]/118mLPotassium chloride — 6 [hp_X]/118mL
Dosage form: Liquid
Route: Oral
Labeler: Talbot's Pharmaceuticals Family Products, LLC.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 20, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Plant Proteins (Chemical structure)Potassium Compounds (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 70797-316_cda1180e-7f69-69b2-e053-2995a90a5015SPL ID cda1180e-7f69-69b2-e053-2995a90a5015SPL set ID 91d57aae-7c68-cc4a-e053-2995a90aad9dUNII 3SW678MX72, A1Y870209Z, 2FXJ6SW4PK, O80TY208ZW, 91GQH8I5F7, XK4IUX8MNB, 2HU33I03UY, 18E7415PXQ, G0R4UBI2ZZ, 660YQ98I10UPC 0370797300066
Pharmacologic class: 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

N470797031601 followed by a unit qualifier and the quantity

Package 70797-0316-01. 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 Oct 5, 2021.

Indications (excerpt from the label)

Uses Uses Temporarily relieves minor aches and pains due to: bruises toothache nerve pain vascular pain nerve pain inflammation and swelling from trauma muscle pain and swelling joint and bone pain Indication

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)