SULPHUR 30C- sulphur liquid

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)

Available from:

Natural Creations, Inc

Administration route:

ORAL

Prescription type:

OTC DRUG

Therapeutic indications:

USES: Temporarily relieves heat and burning in the eyes.** USES: Temporarily relieves heat and burning in the eyes.**

Authorization status:

unapproved homeopathic

Summary of Product characteristics

SULPHUR 30C- SULPHUR LIQUID
NATURAL CREATIONS, INC
_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._
----------
SULPHUR 30C
ACTIVE INGREDIENTS (HPUS*): Sulphur 30C
USES: Temporarily relieves heat and burning in the eyes.**
USES: Temporarily relieves heat and burning in the eyes.**
DIRECTIONS: Adults & children above 12 years: 10 drops orally 3 times
daily, or as
directed by a health care professional.
KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental
ingestion) get medical help or contact a Poison Control Center right
away.
WARNINGS:
Consult a physician for use in children under 12 years of age.
IF PREGNANT OR BREAST-FEEDING, ask a health care professional before
use.
KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental
ingestion) get medical help or contact a Poison Control Center right
away.
Do not use if TAMPER EVIDENT seal is broken or missing.
INACTIVE INGREDIENTS: Ethyl Alcohol USP, Purified Water
QUESTIONS & COMMENTS?
Natural Creations, Inc. / Woodbine, IA 51579 / 712-647-1600
*The letters "HPUS" indicate the components in the product are
officially monographed
in the Homeopathic Pharmacopeia of the United States.
**Claims based on traditional homeopathic practice, not accepted
medical evidence. Not
FDA evaluated.
NDC:43406-0472-1
Sulphur 30C
HOMEOPATHIC
1 fl oz (30mL) / 20% Alcohol
SULPHUR 30C
sulphur liquid
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:43406-0472
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)
SULFUR
30 [hp_C] in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)
PACKAGING
# ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:43406-
0472-1
30 mL in 1 BOTTLE, DROPPER; Type 0: Not a
Combination Pro