Kraj: Stany Zjednoczone
Język: angielski
Źródło: NLM (National Library of Medicine)
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)
Energique, Inc.
ORAL
OTC DRUG
Sulphur 30C - itching** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. May temporarily relieve red, burning, itching skin.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
unapproved homeopathic
SULPHUR 30C- SULPHUR LIQUID ENERGIQUE, 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._ ---------- DRUG FACTS: ACTIVE INGREDIENT: (IN EACH DROP): Sulphur 30C 100% PURPOSE: Sulphur 30C - itching** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. USES: May temporarily relieve red, burning, itching skin.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. WARNINGS: STOP USE AND ASK A DOCTOR IF symptoms persist for more than 7 days. IF PREGNANT OR BREAST-FEEDING, ask a health professional before use. KEEP OUT OF REACH OF CHILDREN. In case of overdose, get medical help or contact a Poison Control Center right away. • Do not use if tamper evident seal is broken or missing. • Store in a cool, dry place. KEEP OUT OF REACH OF CHILDREN: In case of overdose, get medical help or contact a Poison Control Center right away. DIRECTIONS: • Adults and children 5 to 10 drops orally, 1 time daily or as otherwise directed by a health care professional. • Consult a physician for use in children under 12 years of age. INACTIVE INGREDIENTS: Demineralized water, 20% Ethanol. QUESTIONS: Dist. by Energique, Inc. 201 Apple Blvd. Woodbine, IA 51579 800-869-8078 PACKAGE LABEL DISPLAY: ENERGIQUE SINCE 1987 HOMEOPATHIC REMEDY SULPHUR 30C 1 FL. OZ. (30ML) SULPHUR 30C sulphur liquid PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:44911-0700 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 Energique, Inc. INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) PACKAGING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:44911- 0700-1 30 mL in 1 BOTTLE, DROP Przeczytaj cały dokument