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  5. NDC Package Code: 70797-312-01 Dr. Talbots Daily Allergy Relief

NDC Package 70797-312-01 Dr. Talbots Daily Allergy Relief

Allium Cepa,Aralia Racemosa,Euphrasia Officinalis,Galphimia Glauca,Histaminum - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
70797-312-01
Package Description:
1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE (70797-312-04)
Product Code:
70797-312
Proprietary Name:
Dr. Talbots Daily Allergy Relief
Non-Proprietary Name:
Allium Cepa, Aralia Racemosa, Euphrasia Officinalis, Galphimia Glauca, Histaminum Hydrochloricum, Luffa Operculata, Pulsatilla, Solidago, Natrum Muriaticum
Substance Name:
Anemone Pulsatilla; Aralia Racemosa Root; Euphrasia Stricta; Galphimia Glauca Flowering Top; Histamine Dihydrochloride; Luffa Operculata Fruit; Onion; Sodium Chloride; Solidago Virgaurea Flowering Top
Usage Information:
Shake before use, natural juice may settleMeasure only with the dosing syringe providedDo not use dosing syringe with other productsOn dosing syringe, weight is specific to productOn dosing syringe, ml = milliliter, lbs = pounds, kgs = kilogramsChildren under 6 months of age, consult a medical professional before using this product.For sudden onset of symptoms: Use every 15 minutes for up to 8 doses until symptoms relieved, then every 2 hours thereafter.Children 6 - 18 lbs or 3 - 8 kgs 1.25 ml every 2 hours, reduce frequency when symptoms improveChildren 19 - 29 lbs or 9 - 13 kgs 2.5 ml every 2 hours, reduce frequency when symptoms improveChildren 30 - 90 lbs or 14 - 41 kgs 5 ml every 2 hours, reduce frequency when symptoms improve
11-Digit NDC Billing Format:
70797031201
Product Type:
Human Otc Drug
Labeler Name:
Talbot's Pharmaceuticals Family Products, Llc.
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ANEMONE PULSATILLA 12 [hp_X]/118mL
  • ARALIA RACEMOSA ROOT 12 [hp_X]/118mL
  • EUPHRASIA STRICTA 12 [hp_X]/118mL
  • GALPHIMIA GLAUCA FLOWERING TOP 12 [hp_X]/118mL
  • HISTAMINE DIHYDROCHLORIDE 12 [hp_X]/118mL
  • LUFFA OPERCULATA FRUIT 12 [hp_X]/118mL
  • ONION 12 [hp_X]/118mL
  • SODIUM CHLORIDE 6 [hp_X]/118mL
  • SOLIDAGO VIRGAUREA FLOWERING TOP 12 [hp_X]/118mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Dietary Proteins - [CS]
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
  • Vegetable Proteins - [CS]
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    07-20-2020
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 70797-312-01?

    The NDC Packaged Code 70797-312-01 is assigned to a package of 1 bottle in 1 carton / 118 ml in 1 bottle (70797-312-04) of Dr. Talbots Daily Allergy Relief, a human over the counter drug labeled by Talbot's Pharmaceuticals Family Products, Llc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 70797-312 included in the NDC Directory?

    Yes, Dr. Talbots Daily Allergy Relief with product code 70797-312 is active and included in the NDC Directory. The product was first marketed by Talbot's Pharmaceuticals Family Products, Llc. on July 20, 2020 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 70797-312-01?

    The 11-digit format is 70797031201. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-270797-312-015-4-270797-0312-01