EUPHRASIA- euphrasia stricta tablet

EUPHRASIA by

Drug Labeling and Warnings

EUPHRASIA by is a Homeopathic medication manufactured, distributed, or labeled by Standard Homeoipathic Commpany, Standard Homeopathic Commpany. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Made according to the
Homeopathic Pharmacopoeia
of the United States since 1903.

Warnings

Do not use if cap band is missing or broken.

If you are pregnant or nursing, consult a licensed health
care professional before using this product.

If symptoms persist for 7 days or worsen,
contact a licensed practitioner.

Keep this and all medicines out of the reach of children.

To be used according to label indications and/or
standard homeopathic indications.

QUESTIONS

Standard Homeopathic Company
Los Angeles, CA 90061
Questions? 800-624-9659

Directions

Adults: Dissolve 4 tablets under tongue 4 times a day.
Children: Consult a healthcare professional

INACTIVE INGREDIENT

In a base of Acacia Gum and Lactose N.F.

ACTIVE INGREDIENT

EUPHRASIA 30X

INDICATIONS & USAGE

EYE IRRITATION, COLD OR HAY FEVER

Principal Display Panel - 250 Tablet Bottle Label

Standard

Homeopathic
Made in the USA Since 1903

NDC # 0360-0171-01

Homeopathic Medicine

EUPHRASIA

30X

EYE IRRITATION, COLD OR

HAY FEVER*

*Claims based on traditional homeopathic

practice, not accepted medical evidence.

Not FDA evaluated.

250 TABLETS

INGREDIENTS AND APPEARANCE

EUPHRASIA 
euphrasia stricta tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0360-0171
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EUPHRASIA STRICTA (UNII: C9642I91WL) (EUPHRASIA STRICTA - UNII:C9642I91WL)	EUPHRASIA STRICTA	30 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
ACACIA (UNII: 5C5403N26O)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	5mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0360-0171-01	250 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/17/1997

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		02/17/1997

Labeler - Standard Homeoipathic Commpany (008316655)

Establishment
Name	Address	ID/FEI	Business Operations
Standard Homeopathic Commpany		008316655	manufacture(0360-0171) , pack(0360-0171) , label(0360-0171)