Land: Vereinigte Staaten
Sprache: Englisch
Quelle: NLM (National Library of Medicine)
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M)
Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)
TOPICAL
OTC DRUG
Antifungal - cures most jock itch (tinea cruris) - relieves symptoms of jock itch including itching, burning and chafing associated with jock itch
OTC monograph final
MICONAZOLE NITRATE- JOCK ITCH SPRAY AEROSOL, SPRAY DOLGENCORP, INC. (DOLLAR GENERAL & REXALL) ---------- REXALL ANTIFUNGAL MICONAZOLE JOCK ITCH POWDER SPRAY TALC-FREE _ACTIVE INGREDIENT_ Miconazole nitrate 2% _PURPOSE_ Antifungal _USES_ cures most jock itch (tinea cruris) relieves symptoms of jock itch including itching, burning and chafing associated with jock itch _WARNINGS_ FOR EXTERNAL USE ONLY. WHEN USING THIS PRODUCT do not get into eyes or mouth use only as directed. Intentional misuse by deliberately concentrating and inhaling contents cans be harmful or fatal. STOP USE AND ASK A DOCTOR IF irritation occurs no improvement within 2 weeks for jock itch KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or contact a Poison Control Center right away. Do not use on children under 2 years of age. Do not use for diaper rash. Do not use on children under 2 years of age unless directed by a doctor. _DIRECTIONS_ wash affected area and dry thoroughly shake can well and spray a thin layer over affected area twice daily (morning and night) supervise children in the use of this product use daily for 2 weeks. If conditions persist, consult a doctor this product is not effective on scalp or nails in case of clogging, clear nozzle under running water _INACTIVE INGREDIENT_ Disteardimonium Hectorite, Isobutane, Kaolin, SD Alcohol 40-B, Zea Mays (Corn) Starch _QUESTIONS?_ Call 1-866-964-0939 PRINCIPAL DISPLAY PANEL REXALL ANTIFUNGAL JOCK ITCH POWDER SPRAY MICONAZOLE NITRATE 2% Cures most jock itch Relieves itching, chafing and burning NET WT 4.6 OZ (130 G) Dolgencorp, Inc. (DOLLAR GENERAL & REXALL) MICONAZOLE NITRATE jock itch spray aerosol, spray PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:55910-841 ROUTE OF ADMINISTRATION TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE 1.3 g in 130 g INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH DISTEARDIMONIUM HECTORITE (UNII: X68 Lesen Sie das vollständige Dokument