NDC 55714-2384 Acne

Antimon. Crud., Arsenicum Alb., Aur. Met., Berber. Aqui., Bovista, Carbo Veg., Causticum, Chelidonium Majus, Dulcamara, Graphites, Hepar Sulph. Calc., Hydrocotyle, Kali Brom., Kali Iod., Ledum, Lycopodium, Nux Vom., Silicea, Sulphur Iod., Zinc. Met., Echinacea, Juglans Regia, Lappa, Taraxacum

NDC Product Code 55714-2384

NDC Code: 55714-2384

Proprietary Name: Acne 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: Antimon. Crud., Arsenicum Alb., Aur. Met., Berber. Aqui., Bovista, Carbo Veg., Causticum, Chelidonium Majus, Dulcamara, Graphites, Hepar Sulph. Calc., Hydrocotyle, Kali Brom., Kali Iod., Ledum, Lycopodium, Nux Vom., Silicea, Sulphur Iod., Zinc. Met., Echinacea, Juglans Regia, Lappa, Taraxacum 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.
    • 55714-2384 - Acne

NDC 55714-2384-0

Package Description: .5 mL in 1 BOTTLE, GLASS

NDC 55714-2384-1

Package Description: 30 mL in 1 BOTTLE, GLASS

NDC 55714-2384-2

Package Description: 50 mL in 1 BOTTLE, GLASS

NDC Product Information

Acne with NDC 55714-2384 is a a human over the counter drug product labeled by Newton Laboratories, Inc.. The generic name of Acne is antimon. crud., arsenicum alb., aur. met., berber. aqui., bovista, carbo veg., causticum, chelidonium majus, dulcamara, graphites, hepar sulph. calc., hydrocotyle, kali brom., kali iod., ledum, lycopodium, nux vom., silicea, sulphur iod., zinc. met., echinacea, juglans regia, lappa, taraxacum. 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.


Acne 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.

  • ANTIMONY TRISULFIDE 15 [hp_X]/mL
  • ARSENIC CATION (3+) 15 [hp_X]/mL
  • GOLD 15 [hp_X]/mL
  • MAHONIA AQUIFOLIUM ROOT BARK 15 [hp_X]/mL
  • GIANT PUFFBALL 15 [hp_X]/mL
  • ACTIVATED CHARCOAL 15 [hp_X]/mL
  • CAUSTICUM 15 [hp_X]/mL
  • CHELIDONIUM MAJUS 15 [hp_X]/mL
  • SOLANUM DULCAMARA TOP 15 [hp_X]/mL
  • GRAPHITE 15 [hp_X]/mL
  • CALCIUM SULFIDE 15 [hp_X]/mL
  • CENTELLA ASIATICA 15 [hp_X]/mL
  • POTASSIUM BROMIDE 15 [hp_X]/mL
  • POTASSIUM IODIDE 15 [hp_X]/mL
  • LEDUM PALUSTRE TWIG 15 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 15 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 15 [hp_X]/mL
  • SILICON DIOXIDE 15 [hp_X]/mL
  • SULFUR IODIDE 15 [hp_X]/mL
  • ZINC 15 [hp_X]/mL
  • ECHINACEA, UNSPECIFIED 6 [hp_X]/mL
  • ENGLISH WALNUT 6 [hp_X]/mL
  • ARCTIUM LAPPA ROOT 6 [hp_X]/mL
  • TARAXACUM OFFICINALE 6 [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)
  • WATER (UNII: 059QF0KO0R)

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.

Acne Product Label Images

Acne 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

Otc - Keep Out Of Reach Of Children Section

Keep out of reach of children.

Otc - Pregnancy Or Breast Feeding Section

If
pregnant or breat-feeding, ask a doctor before use.

Warnings Section

WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms persist for more than a few days, consult a doctro. If
pregnant or breast-feeding, ask a doctor before use.

Questions

Newtonlabs.net - Questions? 800 448-7256
Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30013

Inactive Ingredient Section

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

Otc - Purpose Section

Formulated for symptoms associated with acne and other skin conditions such as boils, pimples, pustules and sebaceous cysts.

Otc - Active Ingredient Section

Equal parts of Echinacea 6x, Juglans regia 6x, Lappa 6x, Taraxacum 6x, Antimon. crud. 15x, Arsenicum alb. 15x, Aur. met. 15x, Berber. aqui. 15x, Bovista 15x, Carbo veg. 15x, Causticum 15x, Chelidonium maj. 15x, Dulcamara 15x, Graphites 15x, Hepar sulph. calc. 15x, Hydrocotyle 15x, Kali brom. 15x, Kali iod. 15x, Ledum 15x, Lycopodium 15x, Nux vom. 15x, Silicea 15x,Sulphur iod. 15x, Zinc. met. 15x.

Dosage & Administration Section

Directions: Ages 12 and up, take 6 drops by mouth (ages 0 to 11, give 3 drops) one to four times daily or as directed by a health professional. Sensitive persons begin with 1 drop and gradually increase to full dose.

Indications & Usage Section

Formulated for symptoms associated with acne and other skin conditions such as boils, pimples, pustules and sebaceous cysts.

* Please review the disclaimer below.

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