NDC 55714-2278 Caffeine Withdrawal

Aconitum Nap., Arg. Nit., Arsenicum Alb., Belladonna, Benzoicum Acidum, Berber. Vulg., Bryonia, Cantharis, Ceanothus, Chelidonium Majus, Chionanthus Virginica, Cinchona, Coffea Cruda, Conium, Gelsemium, Ignatia, Iris Versicolor, Mezereum, Nux Vom., Passiflora, Pulsatilla, Rhus Toxicodendron, Scutellaria Lateriflora, Staphysag., Chamomilla, Taraxacum, Valeriana

NDC Product Code 55714-2278

NDC Code: 55714-2278

Proprietary Name: Caffeine Withdrawal What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Aconitum Nap., Arg. Nit., Arsenicum Alb., Belladonna, Benzoicum Acidum, Berber. Vulg., Bryonia, Cantharis, Ceanothus, Chelidonium Majus, Chionanthus Virginica, Cinchona, Coffea Cruda, Conium, Gelsemium, Ignatia, Iris Versicolor, Mezereum, Nux Vom., Passiflora, Pulsatilla, Rhus Toxicodendron, Scutellaria Lateriflora, Staphysag., Chamomilla, Taraxacum, Valeriana What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.


Code Structure
  • 55714 - Newton Laboratories, Inc.
    • 55714-2278 - Caffeine Withdrawal

NDC 55714-2278-0

Package Description: .5 mL in 1 BOTTLE, GLASS

NDC 55714-2278-1

Package Description: 29.57 mL in 1 BOTTLE, GLASS

NDC 55714-2278-2

Package Description: 59.14 mL in 1 BOTTLE, GLASS

NDC Product Information

Caffeine Withdrawal with NDC 55714-2278 is a a human over the counter drug product labeled by Newton Laboratories, Inc.. The generic name of Caffeine Withdrawal is aconitum nap., arg. nit., arsenicum alb., belladonna, benzoicum acidum, berber. vulg., bryonia, cantharis, ceanothus, chelidonium majus, chionanthus virginica, cinchona, coffea cruda, conium, gelsemium, ignatia, iris versicolor, mezereum, nux vom., passiflora, pulsatilla, rhus toxicodendron, scutellaria lateriflora, staphysag., chamomilla, taraxacum, valeriana. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Newton Laboratories, 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.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.


Caffeine Withdrawal Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ACONITUM NAPELLUS 15 [hp_X]/mL
  • SILVER NITRATE 15 [hp_X]/mL
  • ARSENIC TRIOXIDE 15 [hp_X]/mL
  • ATROPA BELLADONNA 15 [hp_X]/mL
  • BENZOIC ACID 15 [hp_X]/mL
  • BERBERIS VULGARIS ROOT BARK 15 [hp_X]/mL
  • BRYONIA ALBA ROOT 15 [hp_X]/mL
  • LYTTA VESICATORIA 15 [hp_X]/mL
  • CEANOTHUS AMERICANUS LEAF 15 [hp_X]/mL
  • CHELIDONIUM MAJUS 15 [hp_X]/mL
  • CHIONANTHUS VIRGINICUS BARK 15 [hp_X]/mL
  • CINCHONA OFFICINALIS BARK 15 [hp_X]/mL
  • ARABICA COFFEE BEAN 15 [hp_X]/mL
  • CONIUM MACULATUM FLOWERING TOP 15 [hp_X]/mL
  • GELSEMIUM SEMPERVIRENS ROOT 15 [hp_X]/mL
  • STRYCHNOS IGNATII SEED 15 [hp_X]/mL
  • IRIS VERSICOLOR ROOT 15 [hp_X]/mL
  • DAPHNE MEZEREUM BARK 15 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 15 [hp_X]/mL
  • PASSIFLORA INCARNATA FLOWERING TOP 15 [hp_X]/mL
  • PULSATILLA VULGARIS 15 [hp_X]/mL
  • TOXICODENDRON PUBESCENS LEAF 15 [hp_X]/mL
  • SCUTELLARIA LATERIFLORA 15 [hp_X]/mL
  • DELPHINIUM STAPHISAGRIA SEED 15 [hp_X]/mL
  • MATRICARIA RECUTITA 3 [hp_X]/mL
  • TARAXACUM OFFICINALE 3 [hp_X]/mL
  • VALERIAN 3 [hp_X]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

* Please review the disclaimer below.

Caffeine Withdrawal Product Label Images

Caffeine Withdrawal Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Indications & Usage Section

Caffeine Withdrawal   Formulated for symptoms associated with caffeine use such as cravings, headache, irritability, restlessness and fatigue.

Dosage & Administration Section

ORAL USE ONLY - SHAKE WELL.   Ages 12 and up, take 6 drops orally (ages 0 to 11, give 3 drops) as needed or as directed by a healthcare professional. Sensitive persons begin with 1 drop and gradually increase to full dose.

Otc - Active Ingredient Section

Aconitum nap. 15x, Arg. nit. 15x, Arsenicum alb. 15x, Belladonna 15x, Benzoicum acidum 15x, Berber. vulg. 15x, Bryonia 15x, Cantharis 15x, Ceanothus 15x, Chelidonium majus 15x, Chionanthus virginica 15x, Cinchona 15x, Coffea cruda 15x, Conium 15x, Gelsemium 15x, Ignatia 15x, Iris versicolor 15x, Mezereum 15x, Nux vom. 15x, Passiflora 15x, Pulsatilla 15x, Rhus toxicodendron 15x, Scutellaria lateriflora 15x, Staphysag. 15x, Chamomilla 3x, Taraxacum 3x, Valeriana 3x.

Otc - Purpose Section

Formulated for symptoms associated with caffeine use such as cravings, headache, irritability, restlessness and fatigue.

Inactive Ingredient Section

Inactive Ingredients: USP Purified Water; USP Gluten-free, non-GMO, organic cane dispensing alcohol 20%.

Questions Section

Www.newtonlabs.net  Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30012Questions?  1.800.448.7256

Warnings Section

Warning: Do not use if tamper - evident seal is broken or missing. Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days. Keep out of reach of children.

Otc - Pregnancy Or Breast Feeding Section

Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days.

Otc - Keep Out Of Reach Of Children Section

Keep out of reach of children.

* Please review the disclaimer below.

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