Certain Dri Clinical Strength Prescription Protection Rollon

Product NDC
69693-734
11-digit product format
696930734
Labeler code
69693
Product ID
69693-734_46a1f92e-4412-3989-e063-6394a90a7038
Type
HUMAN OTC DRUG
Nonproprietary name
Certain Dri Clinical Strength Prescription Protection Rollon
Dosage form
LIQUID
Route
TOPICAL
Labeler
Clarion Brands LLC
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-12-24
Substance
ALUMINUM CHLORIDE
Active strength
15 g/100mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Certain Dri Clinical Strength Prescription Protection Rollon
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALUMINUM CHLORIDE15 g/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii3CYT62D3GA

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69693-734-12Certain Dri Clinical Strength Prescription Protection Rollon1 in 1 CARTONLIQUID11
69693-734-12Certain Dri Clinical Strength Prescription Protection Rollon35 mL in 1 CYLINDERLIQUID351

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
69693-734-12696930734121 CYLINDER in 1 CARTON (69693-734-12) / 35 mL in 1 CYLINDER1 cylinder2025-12-24NoNoHistorical