LEDUM PALUSTRE- ledum pal tablet

LEDUM PALUSTRE by

Drug Labeling and Warnings

LEDUM PALUSTRE by is a Homeopathic medication manufactured, distributed, or labeled by STANDARD HOMEOPATHIC COMPANY. 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.

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

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

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

LEDUM PAL. 6X

INDICATIONS & USAGE

BITES OR STINGS

Principal Display Panel -- 250 Tablet Bottle Label

Standard

Homeopathic

Made in the USA Since 1903

NDC # 0360-0252-01

Homeopathic Medicine

LEDUM PAL.

6X

BITES OR STINGS*

*Claims based on traditional homeopathic

practice, not accepted medical evidence.

Not FDA evaluated.

250 TABLETS

INGREDIENTS AND APPEARANCE

LEDUM PALUSTRE 
ledum pal tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0360-0252
Route of Administration	SUBLINGUAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P) (LEDUM PALUSTRE TWIG - UNII:877L01IZ0P)	LEDUM PALUSTRE TWIG	6 [hp_X]  in 1 g

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

Product Characteristics
Color	white	Score	score with uneven pieces
Shape	ROUND	Size	5mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0360-0252-01	1 g 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 HOMEOPATHIC COMPANY (008316655)

Establishment
Name	Address	ID/FEI	Business Operations
STANDARD HOMEOPATHIC COMPANY		008316655	manufacture(0360-0252) , pack(0360-0252) , label(0360-0252)