SULPHUR 7138- sulphur liquid

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

Sulphur 6X, 9X, 12X, 30X

Available from:

Professional Complementary Health Formulas

Administration route:

ORAL

Prescription type:

OTC DRUG

Therapeutic indications:

Use according to standard homeopathic indications for self-limiting conditions. Common Materia Medica indications: dry, scaly or itchy skin, indigestion, vomiting, diarrhea.* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Authorization status:

unapproved homeopathic

Summary of Product characteristics

SULPHUR 7138- SULPHUR LIQUID
PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS
_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._
----------
DSUL
ACTIVE INGREDIENTS
Sulphur 6X, 9X, 12X, 30X
QUESTIONS
Professional Formulas
PO Box 2034 Lake Oswego, OR 97035
INDICATIONS
Use according to standard homeopathic indications for self-limiting
conditions. Common
Materia Medica indications: dry, scaly or itchy skin, indigestion,
vomiting, diarrhea.*
*Claims based on traditional homeopathic practice, not accepted
medical evidence. Not
FDA evaluated.
WARNINGS
In case of overdose, get medical help or contact a poison control
center right away.
Keep out of the reach of children.
If pregnant or breastfeeding, ask a healthcare professional before
use.
DIRECTIONS
Place drops under tongue 30 minutes before/after meals. Adults and
children 12 years
and over: Take 10 drops up to 3 times per day. Consult a physician for
use in children
under 12 years of age.
OTHER INFORMATION
Tamper resistant. If seal is broken, do not use. After opening, close
container tightly and
store at room temperature away from heat.
INACTIVE INGREDIENTS
20% ethanol, purified water.
LABEL
Est 1985
Professional Formulas
Complementary Health
Sulphur
Homeopathic Remedy
1 FL. OZ. (29.5 mL)
SULPHUR 7138
sulphur liquid
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:63083-7138
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)
SULFUR
6 [hp_X] in 29.5 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)
Professional Complementary Health Formulas
PACKAGING
# ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:63083-
7138-1
29.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a
Combination Product
08/15/1985
MARKETING INFORMATION
MARKETING
CA