FDA.reportPublic FDA data

CLEAR MED

Manufacturer
CONTROL CORRECTIVE SKINCARE INC
Effective date
2025-12-31
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 01:30:23

Label at a glance#

ProductCLEAR MED 10%
Active ingredientBENZOYL PEROXIDE
Label structure9 sections

Dosage and administration

ALWAYS PATCH TEST A SMALL AREA BEFORE FIRST APPLICATION. APPLY SPARINGLY TO AFFECTED AREAS ONCE OR TWICE DAILY AS NEEDED, AVOIDING THE EYE AREA. DRYNESS AND LIGHT PEELING MAY OCCUR DURING THE FIRST FEW WEEKS OF USAGE.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

BENZOYL PEROXIDE 10%

PURPOSE

OTC - PURPOSE SECTION

ACNE TREATMENT

USE

INDICATIONS & USAGE SECTION

HELPS REDUCE ACNE BREAKOUTS.

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY. DO NOT USE IF YOU ARE ALLERGIC OR SENSITIVE TO BENZOYL PEROXIDE. WHEN USING THIS PRODUCT AVOID CONTACT WITH EYES, LIPS AND MOUTH. IF CONTACT OCCURS, FLUSH THOROUGHLY WITH WATER. AVOID UNNECESSARY SUN EXPOSURE. MAY BLEACH FABRIC. MILD IRRITATION MAY BE REDUCED BY USING THE PRODUCT LESS FREQUENTLY OR IN A LOWER CONCENTRATION. DISCONTINUE USE, IF IRRITATION OCCURS AND CONSULT YOUR DOCTOR. USING OTHER TOPICAL ACNE MEDICATION AT THE SAME TIME OR IMMEDIATELY FOLLOWING USE OF THIS PRODUCT MAY INCREASE DRYNESS OR IRRITATION OF THE SKIN.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

ALWAYS PATCH TEST A SMALL AREA BEFORE FIRST APPLICATION. APPLY SPARINGLY TO AFFECTED AREAS ONCE OR TWICE DAILY AS NEEDED, AVOIDING THE EYE AREA. DRYNESS AND LIGHT PEELING MAY OCCUR DURING THE FIRST FEW WEEKS OF USAGE.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

WATER, SULFUR 3%, BUTYLENE GLYCOL, CARBOMER, POTASSIUM SORBATE, PHENOXYETHANOL, SODIUM BENZOATE, SODIUM HYDROXIDE.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b UC_Clear Med 10pct01b UC_Clear Med 10pct

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
106310benzoyl peroxide 10 % Topical LotionPSN8
106310benzoyl peroxide 100 MG/ML Topical LotionSCD8
106310benzoyl peroxide 10 % Topical LotionSY8

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
a46239a7-5963-4008-8cbb-6b9000f497ebProduct name120250721
b382b4e1-6b48-45f6-bffc-e61b00b0ce19Product name320250317
d9d61457-6a5a-41fc-b418-e5479a2904b7Product name220230303
32012d5c-25ac-49c7-9d4c-1313177fff7cProduct name120230112
13e7e7e3-e885-4c79-af6d-dad1aedbb06eProduct name120220128
4a7d44fe-774d-404b-aad0-8a90fe78375aProduct name420211025
3f45980c-c196-47e5-0e5e-48b7c57327c5Product name520200428
d12e2d7c-bd6b-45d4-94f9-6df8e1b8b27bProduct name320200203
ee5c6de5-d9cd-454f-b250-7b19e5cf2992Product name420190619
ad75fcfd-a339-42a1-9c60-43ba2c654cfaProduct name120170810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70764-107-512025-12-31C16284748780-12cef2736-8292-d83d-e063-dadaa90ab31fCONTROL CORRECTION - CLEAR MED 10% (70764-107)
70764-107-512025-01-30C16284748780-12cef2736-8292-d83d-e063-dadaa90ab31fCONTROL CORRECTION - CLEAR MED 10% (70764-107)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70764-107-11CLEAR MED10%74 mL in 1 TUBELOTION748
70764-107-51CLEAR MED10%1 in 1 BOXLOTION18

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70764-10770764-107-11, 70764-107-51

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SULFUR70FD1KFU70IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
CARBOMER COPOLYMER TYPE A71DD5V995LIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
PHENOXYETHANOLHIE492ZZ3TIACT
SODIUM BENZOATEOJ245FE5EUIACT
SODIUM HYDROXIDE55X04QC32IIACT
BENZOYL PEROXIDEW9WZN9A0GMACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CLEAR MED 10%BENZOYL PEROXIDECONTROL CORRECTIVE SKINCARE INC7acd1404-2af7-4ec4-b1e9-a905c9f823b82025-12-31WarningsExact identifier
ndc (package): 70764-107-51
ndc (package): 70764-107-11
ndc (product): 70764-107
ndc11 (package): 70764010751
ndc11 (package): 70764010711
spl id: 474ba495-afdc-f075-e063-6394a90a3637
spl set id: 7acd1404-2af7-4ec4-b1e9-a905c9f823b8

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.