NDC Package 70797-308-01 Dr. Talbots Infant Daily Allergy Relief

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

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:
70797-308-01
Package Description:
1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE (70797-308-04)
Product Code:
Proprietary Name:
Dr. Talbots Infant 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:
UsesTemporarily relieves the symptoms associated with hay fever or other upper respiratory allergies, such assneezing sinus pain runny nose watery eyes mild wheezing itchy nose and throat
11-Digit NDC Billing Format:
70797030801
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.
  • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    06-01-2021
    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 70797-308-01?

    The NDC Packaged Code 70797-308-01 is assigned to a package of 1 bottle in 1 carton / 118 ml in 1 bottle (70797-308-04) of Dr. Talbots Infant 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 70797-308 included in the NDC Directory?

    Yes, Dr. Talbots Infant Daily Allergy Relief with product code 70797-308 is active and included in the NDC Directory. The product was first marketed by Talbot's Pharmaceuticals Family Products, Llc on June 01, 2021 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 70797-308-01?

    The 11-digit format is 70797030801. 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
    5-3-270797-308-015-4-270797-0308-01