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  5. NDC Package Code: 49726-048-60 Synaptol Lactose Free

NDC Package 49726-048-60 Synaptol Lactose Free

Aconitum Ferox,Adrenalinum,Aesculus Hippocastanum,Flos,Apis Mellifica,Argentum - 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:
49726-048-60
Package Description:
60 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC
Product Code:
49726-048
Proprietary Name:
Synaptol Lactose Free
Non-Proprietary Name:
Aconitum Ferox, Adrenalinum, Aesculus Hippocastanum, Flos, Apis Mellifica, Argentum Nitricum, Avena Sativa, Baptisia Tinctoria, Cochlearia Armoracia, Phosphorus, Scleranthus Annuus, Flos, Scutellaria Lateriflora, Sumbul, Viola Odorata
Substance Name:
Aconitum Ferox Root; Aesculus Hippocastanum Flower; Apis Mellifera; Avena Sativa Flowering Top; Baptisia Tinctoria Root; Epinephrine; Ferula Sumbul Root; Horseradish; Phosphorus; Scleranthus Annuus Flowering Top; Scutellaria Lateriflora Whole; Silver Nitrate; Viola Odorata Whole
Usage Information:
30 sec. under tongue, then swallow with water.30-50lb (13.6kg-22.6kg): 1/2 tablet twice daily.50lb+ (22.6kg): 1 tablet twice daily.
11-Digit NDC Billing Format:
49726004860
Product Type:
Human Otc Drug
Labeler Name:
Hellolife, Inc.
Dosage Form:
Tablet, Orally Disintegrating - A solid dosage form containing medicinal substances which disintegrates rapidly, usually within a matter of seconds, when placed upon the tongue.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ACONITUM FEROX ROOT 10 [hp_X]/1
  • AESCULUS HIPPOCASTANUM FLOWER 10 [hp_X]/1
  • APIS MELLIFERA 10 [hp_X]/1
  • AVENA SATIVA FLOWERING TOP 10 [hp_X]/1
  • BAPTISIA TINCTORIA ROOT 10 [hp_X]/1
  • EPINEPHRINE 10 [hp_X]/1
  • FERULA SUMBUL ROOT 10 [hp_X]/1
  • HORSERADISH 10 [hp_X]/1
  • PHOSPHORUS 10 [hp_X]/1
  • SCLERANTHUS ANNUUS FLOWERING TOP 10 [hp_X]/1
  • SCUTELLARIA LATERIFLORA WHOLE 10 [hp_X]/1
  • SILVER NITRATE 10 [hp_X]/1
  • VIOLA ODORATA WHOLE 10 [hp_X]/1
    • Pharmacologic Class(es):
  • Adrenergic alpha-Agonists - [MoA] (Mechanism of Action)
  • Adrenergic beta-Agonists - [MoA] (Mechanism of Action)
  • Allergens - [CS]
  • Bee Venoms - [CS]
  • Catecholamine - [EPC] (Established Pharmacologic Class)
  • Catecholamines - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Dietary Proteins - [CS]
  • Food Additives - [CS]
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Increased IgG Production - [PE] (Physiologic Effect)
  • Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Plant Proteins - [CS]
  • Standardized Insect Venom Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • alpha-Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
  • beta-Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    09-27-2022
    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 49726-048-60?

    The NDC Packaged Code 49726-048-60 is assigned to a package of 60 tablet, orally disintegrating in 1 bottle, plastic of Synaptol Lactose Free, a human over the counter drug labeled by Hellolife, Inc.. The product's dosage form is tablet, orally disintegrating and is administered via oral form.

    Is NDC 49726-048 included in the NDC Directory?

    Yes, Synaptol Lactose Free with product code 49726-048 is active and included in the NDC Directory. The product was first marketed by Hellolife, Inc. on September 27, 2022 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 49726-048-60?

    The 11-digit format is 49726004860. 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
    5-3-249726-048-605-4-249726-0048-60