Label: CERTAIN DRI CLINICAL STRENGTH ROLL ON- aluminum chloride for solution
- NDC Code(s): 69693-724-12
- Packager: Clarion Brands, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 1, 2024
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Warnings
- Do not use
- ASK DOCTOR
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Inactive ingredients
- QUESTIONS
-
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
CERTAIN
DRI®
CLINICAL STRENGTH
PRESCRIPTION
PROTECTION
72 Hour
#1 DOCTOR
RECOMENDED*
Most effective
antiperspirant you can buy
without a prescription
ROLL-ON
ANTIPERSPIRANT
ALUMINUM CHLORIDE 15% 1.2 FL OZ (35 mL)
#1 DOCTOR
RECOMMENDED
Clinical Strength Brand*
NEW
LOOK!
Same
trusted
protection!
Satisfaction
Guaranteed.
If you're not completely
satisfied, we will replace or
refund your purchase.
If you have any questions,
visit www.certaindri.com
or call 1-844-923-7837
*Data on file
Formulated with the most
effective antiperspirant you
can buy without a prescription
to help stop excessive sweating
for up to 72 hours.
Stop sweat before it
starts with the same active
ingredient in many prescription
strength formulas - perfect for
excessive sweating - commonly
called hyperhidrosis.
for Maximum Protection:
- Be sure your underarm
is completely dry prior to
application - Apply to each underarm
before bed - Apply Certain Dri® Everyday
Protection each day in the
morning
Learn more at
certaindri.com
1000182
CRUELTY FREE
Distributed by: Certain Dri LLC
811 Broad Street, Suite 600
Chattanooga, TN 37402 ©2023
1000191
- Be sure your underarm
-
INGREDIENTS AND APPEARANCE
CERTAIN DRI CLINICAL STRENGTH ROLL ON
aluminum chloride for solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69693-724 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Aluminum Chloride (UNII: 3CYT62D3GA) (Aluminum Cation - UNII:3XHB1D032B) Aluminum Chloride .15 g in 100 mL Inactive Ingredients Ingredient Name Strength Aloe (UNII: V5VD430YW9) Artemisia Vulgaris Whole (UNII: JDR81QW9ZQ) Glycerin (UNII: PDC6A3C0OX) Cetyl Hydroxyethylcellulose (350000 Mw) (UNII: T7SWE4S2TT) Laminaria Digitata (UNII: 15E7C67EE8) Opuntia Ficus-Indica Flower (UNII: 83YSP51SMA) Polyacrylate-1 Crosspolymer (UNII: R5P9Z5WD6D) Potassium Hydroxide (UNII: WZH3C48M4T) Saccharomyces Cerevisiae (UNII: 978D8U419H) Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69693-724-12 1 in 1 CARTON 02/01/2024 1 35 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M019 02/01/2024 Labeler - Clarion Brands, LLC (079742703)