NDC codes

FDA NDC Directory
Product NDC (as listed)70797-308Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70797-0308Add 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 NDC11-digit (billing)PackageCopy
70797-308-0170797030801707970308011 BOTTLE in 1 CARTON (70797-308-01) / 118 mL in 1 BOTTLE (70797-308-04)Marketed from Jun 1, 2021

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

Generic name (nonproprietary)
allium cepa, aralia racemosa, euphrasia officinalis, galphimia glauca, histaminum hydrochloricum, luffa operculata, pulsatilla, solidago, natrum muriaticum
Active ingredients
Luffa operculata fruit — 12 [hp_X]/118mLEuphrasia stricta — 12 [hp_X]/118mLGalphimia glauca flowering top — 12 [hp_X]/118mLAralia racemosa root — 12 [hp_X]/118mLSolidago virgaurea flowering top — 12 [hp_X]/118mLSodium chloride — 6 [hp_X]/118mLOnion — 12 [hp_X]/118mLAnemone pulsatilla — 12 [hp_X]/118mLHistamine dihydrochloride — 12 [hp_X]/118mL
Dosage form
Liquid
Route
Oral
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
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 70797-308_c0963200-67de-6349-e053-2a95a90adde1SPL ID c0963200-67de-6349-e053-2a95a90adde1SPL set ID c0963200-67dd-6349-e053-2a95a90adde1UNII C4MO6809HU, C9642I91WL, 93PH5Q8M7E, T90W4582DU, 5405K23S50, 451W47IQ8X, 492225Q21H, I76KB35JEV, 3POA0Q644UUPC 0370797300080
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

N470797030801 followed by a unit qualifier and the quantity

Package 70797-0308-01. 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 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 Uses

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70797-308

What is NDC 70797-308?
70797-308 is the product NDC for Dr. Talbots Infant Daily Allergy Relief, Luffa operculata fruit 12 [hp_X]/118mL + 8 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 Infant Daily Allergy Relief (Allium cepa, Aralia racemosa, Euphrasia officinalis, Galphimia glauca, Histaminum hydrochloricum, Luffa operculata, Pulsatilla, Solidago, Natrum muriaticum).
What is the active ingredient?
Luffa operculata fruit, Euphrasia stricta, Galphimia glauca flowering top, Aralia racemosa root, Solidago virgaurea flowering top, Sodium chloride, Onion, Anemone pulsatilla, Histamine dihydrochloride.
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 Infant Daily Allergy Relief?
1 other product NDC are listed under this name. See all Dr. Talbots Infant Daily Allergy Relief NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Dr. Talbots Infant Daily Allergy Relief NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Dr Talbots Infant Daily Allergy Reliefallium cepa 12x,aralia racemosa 12x,euphrasia officinalis 12x,galphimia glauca 12x,histaminum hydrochloricum 12x,luffa operculata 12x,pulsatilla 12x,solidago 12x,natrum muriaticum 6xAralia racemosa root 12 [hp_X]/118mL + 8 more ingredientsLiquidOralTalbot's Pharmaceuticals Family Products,LLC.70797-32270797-0322-01

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