Dr Talbots Infant Mucus Cold Relief NDC 70797-320

NDC codes

FDA NDC Directory

Product NDC (as listed)70797-320Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70797-0320Add 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
70797-320-01	70797032001	1 BOTTLE in 1 CARTON (70797-320-01) / 118 mL in 1 BOTTLEMarketed from Sep 12, 2022

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 Infant Mucus Cold Relief
Generic name (nonproprietary): eupatorium perf 12x,hepar sulphuris calcareum 12x,kali bichromicum 12x,marrubium vulgare 12x,phosphorus 30x,pulsatilla 12x,rumex crispus 12x,sambucus nigra 12x,calcarea sulphurica 12x,ferrum phosphoricum 12x
Active ingredients: Marrubium vulgare — 12 [hp_Q]/118mLSambucus nigra flowering top — 12 [hp_X]/118mLCalcium sulfate anhydrous — 12 [hp_X]/118mLPotassium chloride — 6 [hp_X]/118mLEupatorium perfoliatum flowering top — 12 [hp_X]/118mLAnemone pulsatilla — 12 [hp_X]/118mLPotassium dichromate — 12 [hp_X]/118mLCalcium sulfide — 12 [hp_X]/118mLFerrosoferric phosphate — 12 [hp_X]/118mLRumex crispus root — 12 [hp_X]/118mLPhosphorus — 30 [hp_X]/118mL
Dosage form: Liquid
Route: Oral
Labeler: Talbots Pharmaceuticals Family Products, LLC.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 12, 2022
Listing expires: Dec 31, 2026
Other FDA classes: Calcium (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)
Identifiers: Product ID 70797-320_e8917c54-f4c3-3427-e053-2995a90adbf2SPL ID e8917c54-f4c3-3427-e053-2995a90adbf2SPL set ID e8917c54-f4c2-3427-e053-2995a90adbf2UNII 7A72MUN24Z, CT03BSA18U, E934B3V59H, 660YQ98I10, 1W0775VX6E, I76KB35JEV, T4423S18FM, 1MBW07J51Q, 91GQH8I5F7, 9N1RM2S62C, 27YLU75U4W
Pharmacologic class: Blood Coagulation Factor; 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

N470797032001 followed by a unit qualifier and the quantity

Package 70797-0320-01. 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 Sep 13, 2022.

Indications (excerpt from the label)

Uses Uses: Temporarily relieves cough and congestion associated with colds mucus in chest mucuy cough runny nose sneezing nasal and sinus congestion Uses

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)