STRAMONIUM 6X

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

DATURA STRAMONIUM (UNII: G6W4F0V8Z3) (DATURA STRAMONIUM - UNII:G6W4F0V8Z3)

Available from:

Standard Homeopathic Company

Administration route:

ORAL

Prescription type:

OTC DRUG

Therapeutic indications:

PURPOSE RESTLESSNESS OR SUN HEADACHE INDICATIONS RESTLESSNESS OR SUN HEADACHE

Authorization status:

unapproved homeopathic

Summary of Product characteristics

STRAMONIUM- STRAMONIUM TABLET
STANDARD HOMEOPATHIC COMPANY
_Disclaimer: This homeopathic product has not been evaluated by the
Food and Drug_
_Administration for safety or efficacy. FDA is not aware of scientific
evidence to support_
_homeopathy as effective._
----------
STRAMONIUM 6X
PURPOSE RESTLESSNESS OR SUN HEADACHE
INDICATIONS RESTLESSNESS OR SUN HEADACHE
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 OUT OF REACH OF CHILDREN Keep this and all medicines out of the
reach of
children.
DIRECTIONS: ADULTS: Dissolve 4 tablets under tongue 4 times a day.
CHILDREN: 2
tablets as above.
INACTIVE INGREDIENT In a base of Acacia Gum and Lactose N.F.
QUESTIONS 800-624-9659
ACTIVE INGREDIENT STRAMONIUM 6X
PRINCIPAL DISPLAY PANEL - 250 TABLET LABEL
Standard Homeopathic
Made in the USA Since 1903
NDC # 0360-0362-01
Homeopathic Medicine
STRAMONIUM
6X
RESTLESSNESS OR SUN HEADACHE
250 TABLETS
STRAMONIUM
stramonium tablet
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:0360-0362
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF
STRENGTH
STRENGTH
DATURA STRAMONIUM (UNII: G6W4F0V8Z3) (DATURA STRAMONIUM -
UNII:G6W4F0V8Z 3)
DATURA
STRAMONIUM
6 [hp_X]
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
ACACIA (UNII: 5C5403N26O)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
PRODUCT CHARACTERISTICS
COLOR
white
SCORE
score with uneven pieces
Standard Homeopathic Company
SHAPE
ROUND
SIZE
5mm
FLAVOR
IMPRINT CODE
CONTAINS
PACKAGING
# ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:0360-
0362-01
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
ho