DRY ORIGNAL FRESH 3.5OZ- aluminum chlorohydrate aerosol, spray

Dry Orignal Fresh 3.5oz by

Drug Labeling and Warnings

Dry Orignal Fresh 3.5oz by is a Otc medication manufactured, distributed, or labeled by Rejoice International Corp., BLUE SEA AEROSOL & DAILY CARE CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Aluminum Chlorohydrate 20.2%

Purpose

Antiperspirant

Uses

Reduces underarm wetness

Warnings

Flammable. Do not use near heat, flame or while smoking. Can cause serious injury or death

Do not use

Do not use on broken or irritated skin. Stop use if rash or irritation develops.

• Keep away from face and mouth to avoid breathing in
• Avoid spraying in eyes. Contents under pressure. Do not puncture or incinerate. Do not expose to heat or store at temperatures above 120ºF/50ºC or enclosed places that could overheat.
• USE ONLY AS DIRECTED. INTENTIONAL MISUSE BY DELIBERATELY CONCENTRATING AND INHALING THE CONTENT CAN BE HARMFUL OR FATAL.

Ask a doctor

Ask a doctor before using, if you have kidney disease.

Keep out of reach of children

Keep out of reach of children

Directions

For undearm use only. Shake can well before each use. Hold can 6 inches away from skin. Spray underarm.

Inactive ingredients

Cyclopentasiloxane

Butane

Propane

Isobutane

Hydrofluorocarbon 152A

PPG-14 Butyl Ether

C12-15 Alkyl Benzoate

Helianthus Annuus (Sunflower) Seed Oil

Fragrance

BHT

Dimethiconol

Disteardimonium Hectorite

Octldodecanol

Propylene Carbonate

Tocopheryl Acetate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DRY ORIGNAL FRESH 3.5OZ 
aluminum chlorohydrate aerosol, spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 57337-152
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	20.2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
DIMETHICONE (UNII: 92RU3N3Y1O)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
PPG-14 BUTYL ETHER (UNII: R199TJT95T)
OCTYLDODECANOL (UNII: 461N1O614Y)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
PROPANE (UNII: T75W9911L6)
BUTANE (UNII: 6LV4FOR43R)
1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
SUNFLOWER OIL (UNII: 3W1JG795YI)
ISOBUTANE (UNII: BXR49TP611)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 57337-152-01	99 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	12/12/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	12/12/2023

Labeler - Rejoice International Corp. (078741245)

Establishment
Name	Address	ID/FEI	Business Operations
BLUE SEA AEROSOL & DAILY CARE CO., LTD.		544373091	manufacture(57337-152)