NDC 68703-094 Styegone

NDC Product Code 68703-094

NDC 68703-094-59

Package Description: 59 mL in 1 BOTTLE, GLASS

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Styegone with NDC 68703-094 is a product labeled by Native Remedies, Llc. The generic name of Styegone is . The product's dosage form is and is administered via form.

Labeler Name: Native Remedies, Llc

Dosage Form: -

Product Type: 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.

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)

Product Labeler Information

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

Labeler Name: Native Remedies, Llc
Labeler Code: 68703
Start Marketing Date: 03-27-2013 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: I 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.

Styegone Product Label Images

Styegone 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 - Purpose

Relieves pain, inflammation and pus

Otc - Active Ingredient

Active Ingredients:Each dose contains equal parts of: Pulsatilla 6C HPUS, Staphysagria 6C HPUS, Psorinum 6C HPUS, Graphites 6C HPUS

Indications & Usage

Uses:Homeopathic remedy temporarily relieves styes

Warnings

Warnings: If symptoms persist or worsen, consult a healthcare professional

Otc - Pregnancy Or Breast Feeding

If pregnant of breastfeeding, ask a health professional before use

Otc - Keep Out Of Reach Of Children

Keep this and all medication out of reach of children

Overdosage

In case of overdose, get medical help or contact a Poison Control Center right away

Dosage & Administration

Directions:For all ages: Mix 0.50 mL drops in 1/4 cup of water and sip slowly. Repeat every 2 hours until symptoms subside

Inactive Ingredient

Inactive Ingredients: USP Purified Water, USP Grain Alcohol 20% by volume

Information For Patients

The letters HPUS indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United StatesAll Native Remedies health products are especially formulated by experts in the field of natural health and are manufactured according to the highest pharmaceutical standards for maximum safety and effectiveness. For more information, visit us at www.nativeremedies.comDistributed byNative Remedies, LLC6531 Park of Commerce Blvd.Suite 160Boca Raton, Fl 33487Phone: +1.877.289.1235International: +1.561.999.8857Contains no animal products, gluten, artificial flavors, preservatives or colorants. Suitable for vegetarians and safe for all ages

Storage And Handling

Tamper resistant for your protection. Use only if safety seal is intact

* Please review the disclaimer below.