Kraj: Stany Zjednoczone
Język: angielski
Źródło: NLM (National Library of Medicine)
ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V) (ALUMINUM SESQUICHLOROHYDRATE - UNII:UCN889409V)
A.P. Deauville, LLC
TOPICAL
OTC DRUG
Reduces underarm wetness.
OTC monograph final
POWER STICK INVISIBLE PROTECTION ROLL- ON ANTIPERSPIRANT DEODORANT SPRING FRESH- ALUMINUM SESQUICHLOROHYDRATE STICK A.P. DEAUVILLE, LLC ---------- POWER STICK INVISIBLE PROTECTION ROLL- ON ANTIPERSPIRANT DEODORANT SPRING FRESH _DRUG FACTS_ _ACTIVE INGREDIENT_ Aluminum Sesquichlorohydrate, 25% _PURPOSE_ Antiperspirant _USE_ Reduces underarm wetness. _WARNINGS_ FOR EXTERNAL UES ONLY. DO NOT USE on broken skin. STOP USE IF rash or irritation occurs ASK A DOCTOR BEFORE USE if you have kidney disease KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or contact a Poison Control Center immediately. QUESTIONS? (732) 719-3475 _DIRECTIONS_ Apply to underams only. _INACTIVE INGREDIENTS_ Water, PPG-14 Butyl Ether, Propylene Glycol, Steareth-2, Cyclopentasiloxane, Fragrance, Steareth-21, PEG-8 Distearate, Citric Acid PACKAGE LABELING: POWER STICK INVISIBLE PROTECTION ROLL- ON ANTIPERSPIRANT DEODORANT SPRING FRESH aluminum sesquichlorohydrate stick PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:42913-039 ROUTE OF ADMINISTRATION TOPICAL A.P. Deauville, LLC ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V) (ALUMINUM SESQUICHLOROHYDRATE - UNII:UCN889409V) ALUMINUM SESQUICHLOROHYDRATE 250 mg in 1 mL INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH WATER (UNII: 059QF0KO0R) PPG-14 BUTYL ETHER (UNII: R199TJT95T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) STEARETH-2 (UNII: V56DFE46J5) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) STEARETH-21 (UNII: 53J3F32P58) PEG-8 DISTEARATE (UNII: 7JNC8VN07M) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) PRODUCT CHARACTERISTICS COLOR white SCORE SHAPE OVAL SIZE FLAVOR IMPRINT CODE CONTAINS PACKAGING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:42913- 039-00 53 mL in 1 CONTAINER; Type 0: Not a Combination Product 01/01/2023 MARKETING INFORMATION MARKETING CATEGORY APPLICATION NUMBER OR MONOGRAPH CITATION MARKETING START DATE MARKETING END DATE OTC Monograph Drug M019 01/01/2023 LABE Przeczytaj cały dokument