LA FRESH ANTIPERSPIRANT WIPE- aluminum chlorohydrate 15% cloth

LA FRESH Antiperspirant Wipe by

Drug Labeling and Warnings

LA FRESH Antiperspirant Wipe by is a Otc medication manufactured, distributed, or labeled by Diamond Wipes International, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Aluminum Chlorohydrate 15%

Purpose

Antiperspirant

Use

reduce underarm perspiration

Warnings

For external use 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

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

Inactive ingredients

Benzoic Acid, Benzyl Alcohol, Chlorphenesin, Fragrance, PEG-180, Phenoxyethanol, Polysorbate 20, Potassium Sorbate, Salvia Officinalis (Sage) Leaf Extract, Sorbic Acid, Tocopherol, Tocopheryl Acetate, Usnea Barbata (Lichen) Extract, Water

Label

LA Fresh®

No Sweat

Anti-perspirant Wipes

Plant- Based Fiber

Controls sweat and smell

Powerful wetness protection

10 WIPES

6' x 7.5'

open here

Do Not Flush

INGREDIENTS AND APPEARANCE

LA FRESH ANTIPERSPIRANT WIPE 
aluminum chlorohydrate 15% cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64709-161
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	0.15 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
SAGE (UNII: 065C5D077J)
USNEA BARBATA (UNII: D6DVA9TCAP)
TOCOPHEROL (UNII: R0ZB2556P8)
WATER (UNII: 059QF0KO0R)
BENZYL ALCOHOL (UNII: LKG8494WBH)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PEG-180 (UNII: Q662QK8M3B)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64709-161-10	36.58 g in 1 PACKET; Type 0: Not a Combination Product	01/31/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	01/31/2025

Labeler - Diamond Wipes International, Inc (161104729)

Registrant - Diamond Wipes International, Inc (161104729)

Establishment
Name	Address	ID/FEI	Business Operations
Diamond Wipes International, Inc		161104729	manufacture(64709-161)