Dr. Talbots Daily Allergy Relief NDC 70797-312

NDC codes

FDA NDC Directory

Product NDC (as listed)70797-312Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70797-0312Add 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
70797-312-01	70797031201	1 BOTTLE in 1 CARTON (70797-312-01) / 118 mL in 1 BOTTLE (70797-312-04)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 Daily Allergy Relief
Generic name (nonproprietary): allium cepa, aralia racemosa, euphrasia officinalis, galphimia glauca, histaminum hydrochloricum, luffa operculata, pulsatilla, solidago, natrum muriaticum
Active ingredients: Aralia racemosa root — 12 [hp_X]/118mLGalphimia glauca flowering top — 12 [hp_X]/118mLLuffa operculata fruit — 12 [hp_X]/118mLEuphrasia stricta — 12 [hp_X]/118mLHistamine dihydrochloride — 12 [hp_X]/118mLAnemone pulsatilla — 12 [hp_X]/118mLOnion — 12 [hp_X]/118mLSodium chloride — 6 [hp_X]/118mLSolidago virgaurea flowering top — 12 [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)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 70797-312_cda1180e-7f6a-69b2-e053-2995a90a5015SPL ID cda1180e-7f6a-69b2-e053-2995a90a5015SPL set ID 91c2795d-4cde-6e2c-e053-2995a90a0096UNII T90W4582DU, 93PH5Q8M7E, C4MO6809HU, C9642I91WL, 3POA0Q644U, I76KB35JEV, 492225Q21H, 451W47IQ8X, 5405K23S50UPC 0370797300028
Pharmacologic class: Non-Standardized Food Allergenic Extract; Osmotic Laxative

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

N470797031201 followed by a unit qualifier and the quantity

Package 70797-0312-01. 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 the symptoms associated with hay fever or other upper respiratory allergies, such as sneezing sinus pain runny nose watery eyes mild wheezing itchy nose and throat Indication

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)