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  5. NDC Package Code: 57955-0261-2 Back, Muscle And Joint Relief

NDC Package 57955-0261-2 Back, Muscle And Joint Relief

Aesculus Hipp,Arnica,Bellis,Bryonia,Calc Carb,Calc Fluor,Cimicifuga,Cobaltum - 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:
57955-0261-2
Package Description:
59 mL in 1 BOTTLE, SPRAY
Product Code:
57955-0261
Proprietary Name:
Back, Muscle And Joint Relief
Non-Proprietary Name:
Aesculus Hipp, Arnica, Bellis, Bryonia, Calc Carb, Calc Fluor, Cimicifuga, Cobaltum Met, Gnaphalium Poly, Hypericum, Kali Carb, Kali Phos, Mag Phos, Oxalicum Ac, Phos, Rhus Tox, Ruta, Zinc Met
Substance Name:
Arnica Montana Whole; Bellis Perennis Whole; Black Cohosh; Bryonia Alba Root; Calcium Fluoride; Cobalt; Dibasic Potassium Phosphate; Horse Chestnut; Hypericum Perforatum Whole; Magnesium Phosphate, Dibasic Trihydrate; Oxalic Acid Dihydrate; Oyster Shell Calcium Carbonate, Crude; Phosphorus; Potassium Carbonate; Pseudognaphalium Obtusifolium Whole; Ruta Graveolens Flowering Top; Toxicodendron Pubescens Leaf; Zinc
Usage Information:
Initially, depress pump untilprimed. Spray one dose directly into mouth.Adults: 3 sprays 3 times per day.Children (6 - 12): 2 sprays 3 times per day.Consult a physician for use in childrenunder 6 years of age.Use additionally asneeded, up to 6 times per day.Reference image: Back.jpg
11-Digit NDC Billing Format:
57955026102
Product Type:
Human Otc Drug
Labeler Name:
King Bio Inc.
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):
  • ARNICA MONTANA WHOLE 10 [hp_X]/59mL
  • BELLIS PERENNIS WHOLE 10 [hp_X]/59mL
  • BLACK COHOSH 10 [hp_X]/59mL
  • BRYONIA ALBA ROOT 10 [hp_X]/59mL
  • CALCIUM FLUORIDE 10 [hp_X]/59mL
  • COBALT 10 [hp_X]/59mL
  • DIBASIC POTASSIUM PHOSPHATE 10 [hp_X]/59mL
  • HORSE CHESTNUT 10 [hp_X]/59mL
  • HYPERICUM PERFORATUM WHOLE 10 [hp_X]/59mL
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 10 [hp_X]/59mL
  • OXALIC ACID DIHYDRATE 10 [hp_X]/59mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 10 [hp_X]/59mL
  • PHOSPHORUS 10 [hp_X]/59mL
  • POTASSIUM CARBONATE 10 [hp_X]/59mL
  • PSEUDOGNAPHALIUM OBTUSIFOLIUM WHOLE 10 [hp_X]/59mL
  • RUTA GRAVEOLENS FLOWERING TOP 10 [hp_X]/59mL
  • TOXICODENDRON PUBESCENS LEAF 10 [hp_X]/59mL
  • ZINC 10 [hp_X]/59mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Inhibition Small Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Magnesium Ion Exchange Activity - [MoA] (Mechanism of Action)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
  • Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
  • Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    02-23-2022
    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 57955-0261-2?

    The NDC Packaged Code 57955-0261-2 is assigned to a package of 59 ml in 1 bottle, spray of Back, Muscle And Joint Relief, a human over the counter drug labeled by King Bio Inc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 57955-0261 included in the NDC Directory?

    Yes, Back, Muscle And Joint Relief with product code 57955-0261 is active and included in the NDC Directory. The product was first marketed by King Bio Inc. on February 23, 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 57955-0261-2?

    The 11-digit format is 57955026102. 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 5-4-1 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
    5-4-157955-0261-25-4-257955-0261-02