Dr Talbots Infant Daily Allergy Relief NDC 70797-322

NDC codes

FDA NDC Directory

Product NDC (as listed)70797-322Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70797-0322Add 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
70797-322-01	70797032201	1 BOTTLE in 1 CARTON (70797-322-01) / 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 Daily Allergy Relief
Generic name (nonproprietary): allium cepa 12x,aralia racemosa 12x,euphrasia officinalis 12x,galphimia glauca 12x,histaminum hydrochloricum 12x,luffa operculata 12x,pulsatilla 12x,solidago 12x,natrum muriaticum 6x
Active ingredients: Aralia racemosa root — 12 [hp_X]/118mLEuphrasia stricta — 12 [hp_X]/118mLLuffa operculata fruit — 12 [hp_X]/118mLOnion — 12 [hp_X]/118mLAnemone pulsatilla — 12 [hp_X]/118mLHistamine dihydrochloride — 12 [hp_X]/118mLSolidago virgaurea flowering top — 12 [hp_X]/118mLGalphimia glauca flowering top — 12 [hp_X]/118mLSodium 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: Sep 12, 2022
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 70797-322_e8bdcc8a-c948-ff5d-e053-2a95a90a3b92SPL ID e8bdcc8a-c948-ff5d-e053-2a95a90a3b92SPL set ID e8bdcc8a-c947-ff5d-e053-2a95a90a3b92UNII T90W4582DU, C9642I91WL, C4MO6809HU, 492225Q21H, I76KB35JEV, 3POA0Q644U, 5405K23S50, 93PH5Q8M7E, 451W47IQ8X
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

N470797032201 followed by a unit qualifier and the quantity

Package 70797-0322-01. 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 12, 2022.

Indications (excerpt from the label)

Uses Temporrarily relieves the symptoms asscociated with hay fever or other upper respiratory allergies, such as itchy nose and throat watery eyes runny nose sneezing sinus pain mild wheezing Uses

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)