NDC 57520-0026 Acneforce

Berberis Vulgaris, Cimicifuga Racemosa, Hydrocotyle Asiatica, Lappa Major, Belladonna, Calcarea Carbonica, Causticum, Eugenia Jambosa,

NDC Product Code 57520-0026

NDC Code: 57520-0026

Proprietary Name: Acneforce 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: Berberis Vulgaris, Cimicifuga Racemosa, Hydrocotyle Asiatica, Lappa Major, Belladonna, Calcarea Carbonica, Causticum, Eugenia Jambosa, 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.

NDC Code Structure

  • 57520 - Apotheca Company
    • 57520-0026 - Acneforce

NDC 57520-0026-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Acneforce with NDC 57520-0026 is a a human over the counter drug product labeled by Apotheca Company. The generic name of Acneforce is berberis vulgaris, cimicifuga racemosa, hydrocotyle asiatica, lappa major, belladonna, calcarea carbonica, causticum, eugenia jambosa,. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Apotheca Company

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.

Acneforce 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.

  • ATROPA BELLADONNA 12 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL
  • SEPIA OFFICINALIS JUICE 12 [hp_X]/mL
  • PALLADIUM 12 [hp_X]/mL
  • CENTELLA ASIATICA 3 [hp_X]/mL
  • BLACK COHOSH 3 [hp_X]/mL
  • BERBERIS VULGARIS ROOT BARK 3 [hp_X]/mL
  • ARCTIUM LAPPA ROOT 3 [hp_X]/mL
  • VIOLA TRICOLOR 12 [hp_X]/mL
  • CAUSTICUM 12 [hp_X]/mL
  • POTASSIUM BROMIDE 12 [hp_X]/mL
  • EUGENIA JAMBOS 12 [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.

  • WATER (UNII: 059QF0KO0R)
  • 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.

Labeler Name: Apotheca Company
Labeler Code: 57520
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 01-28-2010 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2018 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: E What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Acneforce Product Label Images

Acneforce 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 - Active Ingredient

Active Ingredients: Berberis Vulgaris 3X, Cimicifuga Racemosa 3X, Hydrocotyle Asiatica 3X, Lappa Major 3X, Belladonna 12X, Calcarea Carbonica 12X, Causticum 12X, Eugenia Jambosa 12X, Kali Bromatum 12X, Palladium Metallicum 12X, Sepia 12X, Viola Tricolor 12X.

Otc - Purpose

Indications:  For temporary relief of eruptions on face and head, and relief of burning and itching.

Warnings

WARNING:  If pregnant or breast-feeding, ask a health care professional before use.Keep out of reach of children.  In case of overdose, get medical help or contact a Poison Control Center right away.Do not use if tamper evident seal is broken or missing.Store in a cool, dry place.

Dosage & Administration

DIRECTIONS:  10 drops orally, 3 times a day.  Consult a physician for use in children under 12 years of age.

Inactive Ingredient

Other Ingredients:  Demineralized Water, 25% Ethanol,

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN:  In case of overdose, get medical help or contact a Poison Control Center right away.

Indications & Usage

INDICATIONS:  For temporary relief of eruptions on face and head, and relief of burning and itching.

Otc - Questions

Distributed by:BIOACTIVE NUTRITIONALMelbourne, FL 32935For Nutritional Information write:BioActive Nutritional, Inc.1803 N. Wickham Rd.Melbourne, FL 32935

* Please review the disclaimer below.

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