ANTIPERSPIRANT WIPE FOR WOMEN- aluminum chlorohydrate swab

Antiperspirant Wipe for Women by

Drug Labeling and Warnings

Antiperspirant Wipe for Women by is a Otc medication manufactured, distributed, or labeled by FlawlessWipes, LLC, Diamond Wipes International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Aluminum Chlorohydrate 15%

Purpose

Antiperspirant

USES

Underarm antiperspirant to reduce perspiration and odor

WARNINGS

• For external use only
• When using this product avoid contact with eyes. in case of eye contact, flush thoroughly with water.
• Discontinue use and contact a doctor if irritation and redness develop and conditions persist for more than 72 hours

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a poison control center right away

DIRECTIONS

Open packet, remove and unfold wipe, apply to underarm only, dispose of used wipe in the trash, do not flush.

Inactive ingredients

Water, polysorbate 20, Salvia Officinalis (Sage) Leaf Extract, Usnea Barbata (Lichen) extract, Tocopherol, Tocopheryl Acetate, PEG-180, Phenoxyethanol, Benzyl Alcohol, Potassium Sorbate, Fragrance

Pakaging

INGREDIENTS AND APPEARANCE

ANTIPERSPIRANT WIPE FOR WOMEN 
aluminum chlorohydrate swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71592-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	15 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
USNEA BARBATA (UNII: D6DVA9TCAP)
TOCOPHEROL (UNII: R0ZB2556P8)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
SAGE (UNII: 065C5D077J)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZYL ALCOHOL (UNII: LKG8494WBH)
POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)

Product Characteristics
Color	white	Score
Shape	RECTANGLE	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71592-001-86	6 in 1 PACKAGE	07/18/2017
1	NDC: 71592-001-85	3 g in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	07/18/2017

Labeler - FlawlessWipes, LLC (080676003)

Registrant - FlawlessWipes, LLC (080676003)

Establishment
Name	Address	ID/FEI	Business Operations
Diamond Wipes International, Inc.		161104729	manufacture(71592-001)