GISELLE ANTIPERSPIRANT DEODORANT ROLL-ON FOR WOMEN- antiperspirant deodorant roll-on for women cream

GISELLE ANTIPERSPIRANT DEODORANT ROLL-ON FOR WOMEN by

Drug Labeling and Warnings

GISELLE ANTIPERSPIRANT DEODORANT ROLL-ON FOR WOMEN by is a Otc medication manufactured, distributed, or labeled by EVI LABS. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ALUMINUM CHLOROHYDRATE 10%

PURPOSE

ANTIPERSPIRANT

USE

REDUCES UNDERARM PERSPIRATION

WARNING

FOR EXTERNAL USE ONLY

DIRECTIONS

Shake well before use. Apply to underarms only. Close tight after use.

INACTIVE INGREDIENTS

Fragrance, Poly aminopropyl Biguanide, PPG-15 Stearyl Ether, Steareth-2, Steareth-21, Water

INDICATIONS & USAGE

Do not use on broken skin.

Stop use if rash or irritation occurs.

DOSAGE & ADMINISTRATION

Apply to underarms only

KEEP OUT OF REACH OF CHILDREN

IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GISELLE ANTIPERSPIRANT DEODORANT ROLL-ON FOR WOMEN 
antiperspirant deodorant roll-on for women cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84178-011
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	8.5 g  in 85 g

Inactive Ingredients
Ingredient Name	Strength
STEARETH-2 (UNII: V56DFE46J5)	3.4 g  in 85 g
PPG-15 STEARYL ETHER (UNII: 1II18XLS1L)	3.4 g  in 85 g
WATER (UNII: 059QF0KO0R)	65.918 g  in 85 g
FRAGRANCE FLORAL ORC0902236 (UNII: R66Z4YW3X0)	1.7 g  in 85 g
POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET)	0.17 g  in 85 g
STEARETH-21 (UNII: 53J3F32P58)	1.913 g  in 85 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84178-011-02	85 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	10/01/2024

Labeler - EVI LABS (123617598)

Establishment
Name	Address	ID/FEI	Business Operations
EVI LABS		123617598	manufacture(84178-011)