CERTAIN DRI- aluminum chlorohydrate cloth

CERTAIN DRI by

Drug Labeling and Warnings

CERTAIN DRI by is a Otc medication manufactured, distributed, or labeled by Clarion Brands, LLC, Diamond Wipes International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

PURPOSE

• Active ingredient (in each wipe): Purpose
• Aluminum chlorohydrate 15%: Antiperspirant

INDICATIONS & USAGE

Use reduces underarm perspiration

Warnings

For external use only

DO NOT USE

Do not use

• on broken or irritated skin
• immediately after shaving

ASK DOCTOR

Ask a doctor before use if you have kidney disease

WHEN USING

When using this product

• do not use in or near eyes
• apply to underarms only

KEEP OUT OF REACH OF CHILDREN

STOP USE

Stop use and ask a doctor if rash or irritation develops

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 offcinalis (sage) leaf extract, sorbic acid, tocopherol, tocopheryl acetate, usnea barbata (lichen) extract, water

QUESTIONS

Questions? call 1-844-923-7837

PRINCIPAL DISPLAY PANEL

CERTAIN
DRI®

CLINICAL STRENGTH

ALUMINUM CHLOROHYDRATE 15%

1 ANTIPERSPIRANT WIPE

SKIN-FRIENDLY INGREDIENTS | DRIES QUICKLY | NO RESIDUE OR STICKINESS

Distributed by: Certain Dri LLC
811 Broad Street, Suite 600
Chattanooga, TN 37402 ©2023

1000166

CRUELTY
FREE

INGREDIENTS AND APPEARANCE

CERTAIN DRI 
aluminum chlorohydrate cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69693-725
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
Benzoic Acid (UNII: 8SKN0B0MIM)
Benzyl Alcohol (UNII: LKG8494WBH)
Chlorphenesin (UNII: I670DAL4SZ)
Polyethylene Glycol 8000 (UNII: Q662QK8M3B)
Phenoxyethanol (UNII: HIE492ZZ3T)
Polysorbate 20 (UNII: 7T1F30V5YH)
Potassium Sorbate (UNII: 1VPU26JZZ4)
Salvia Officinalis Flowering Top (UNII: 48JCS720FN)
Sorbic Acid (UNII: X045WJ989B)
Tocopherol (UNII: R0ZB2556P8)
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)
Usnea Barbata (UNII: D6DVA9TCAP)
Water (UNII: 059QF0KO0R)

Product Characteristics
Color	WHITE (TOWLETTE PRE-MOISTENED WITH ANTIPERSPIRANT LIQUID)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69693-725-06	30 g in 1 PACKET; Type 0: Not a Combination Product	10/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M019	10/01/2023

Labeler - Clarion Brands, LLC (079742703)