CLEAR MED

Product NDC: 70764-106
11-digit product format: 707640106
Labeler code: 70764
Product ID: 70764-106_474bae9f-b921-2d83-e063-6394a90abd27
Type: HUMAN OTC DRUG
Nonproprietary name: BENZOYL PEROXIDE
Dosage form: LOTION
Route: TOPICAL
Labeler: CONTROL CORRECTIVE SKINCARE INC
Application: M006
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2016-06-09
Substance: BENZOYL PEROXIDE
Active strength: 5 g/100mL
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 18 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	70764-106-51	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	70764-106-51	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	70764-106-51	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	70764-106-51	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	70764-106-51	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	70764-106-51	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	70764-106-51	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	70764-106-51	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	70764-106-51	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: CLEAR MED
Brand name suffix: 5%
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BENZOYL PEROXIDE	5 g/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
W9WZN9A0GM	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
106309	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
03799b2c-cab1-4672-9004-29e4873d022f	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
a46239a7-5963-4008-8cbb-6b9000f497eb	Product name	1	20250721
b382b4e1-6b48-45f6-bffc-e61b00b0ce19	Product name	3	20250317
d9d61457-6a5a-41fc-b418-e5479a2904b7	Product name	2	20230303
32012d5c-25ac-49c7-9d4c-1313177fff7c	Product name	1	20230112
13e7e7e3-e885-4c79-af6d-dad1aedbb06e	Product name	1	20220128
c6f86816-7da6-43ea-8c25-ac9758311cc5	Product name	1	20220118
4a7d44fe-774d-404b-aad0-8a90fe78375a	Product name	4	20211025
3c386306-c48a-413e-bb69-70cb268496f3	Product name	1	20210727
3f45980c-c196-47e5-0e5e-48b7c57327c5	Product name	5	20200428
d12e2d7c-bd6b-45d4-94f9-6df8e1b8b27b	Product name	3	20200203
ee5c6de5-d9cd-454f-b250-7b19e5cf2992	Product name	4	20190619
ad75fcfd-a339-42a1-9c60-43ba2c654cfa	Product name	1	20170810
252e11b6-1a9a-4283-a242-df2c129c496d	Product name	3	20170717

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70764-106-51	2025-12-31	C162847	48780-1	2cef2736-ae36-d83d-e063-dadaa90ab31f	CONTROL CORRECTIVE - CLEAR MED 5% (70764-106)
70764-106-51	2025-01-30	C162847	48780-1	2cef2736-ae36-d83d-e063-dadaa90ab31f	CONTROL CORRECTIVE - CLEAR MED 5% (70764-106)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70764-106-11	CLEAR MED5%	74 mL in 1 TUBE	LOTION	74		10
70764-106-51	CLEAR MED5%	1 in 1 BOX	LOTION	1		10

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70764-106	CLEAR MED 5% (BENZOYL PEROXIDE) LOTION [CONTROL CORRECTIVE SKINCARE INC]	9	Current NDC, Legacy NDC, 2 package rows	20230923_03799b2c-cab1-4672-9004-29e4873d022f.zip

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 20 of 55 · 1,088 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Dermaharmony 10% Sulfur	SULFUR	D3 Development, Inc.	c78ead80-a8ee-0b52-e053-2a95a90ab880	2025-12-01	Warnings	Exact identifier application number: M006
Dermaharmony 10% Sulfur with Tea Tree Oil	SULFUR	D3 Development, Inc.	c79005d4-0c6f-75d0-e053-2995a90a8314	2025-12-01	Warnings	Exact identifier application number: M006
Resurfacing acne swipes	SALICYLIC ACID	Oars And Alps LLC	efe14f46-c947-aea4-e053-2a95a90aad5f	2025-12-01	Warnings	Exact identifier application number: M006
EradiKate ACNE TREATMENT	SULFUR	Rare Beauty Brands Inc	44ebacf3-52c1-4896-e063-6394a90ac447	2025-12-01	Warnings	Exact identifier application number: M006
EradiKate Daily Foaming Cleanser Acne Treatment	SULFUR	Rare Beauty Brands Inc.	44ebc725-796f-71e6-e063-6294a90a69a6	2025-12-01	Warnings	Exact identifier application number: M006
ERADIKATE ACNE MARK FADING	SALICYLIC ACID	Rare Beauty Brands Inc.	44ebe505-1ce8-88cf-e063-6394a90a4baf	2025-12-01	Warnings	Exact identifier application number: M006
Jane Seymour Natural Advantage AM SPF 15 All Day Moisture with AHAs	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE	Guthy-Renker,LLC	76298090-e873-4307-8bdb-19cdab6d9ac2	2025-12-01	Warnings	Exact identifier application number: M006
Asepxia Baking Soda Acne Bar	SALICYLIC ACID	Genomma Lab USA	ded9fe59-9477-4425-8bbb-f9a49118f004	2025-12-01	Warnings	Exact identifier application number: M006
Blemish Buster Solution Acne Treatment	SULFUR	Guthy-Renker LLC	d2b9462d-7897-40a4-9022-eeb04e7d5adf	2025-12-01	Warnings	Exact identifier application number: M006
Anna Guanche MD Miracle Cream The Pimple Cream	SULFUR	Bella Cosmeceuticals, Inc.	b4562cf4-aae3-e9db-e053-2995a90a7210	2025-11-30	Warnings	Exact identifier application number: M006
Vanishing Skincare	VANISHING DRY SERUM MASK, PHASE 3	Vanish Skincare LLC	27f19c03-1a18-6c74-e063-6394a90a6e86	2025-11-28	Warnings	Exact identifier application number: M006
OUHOE CLEARFACE Overnight Acne	SALICYLIC ACID	Shantou Ouhoe Technology Co., Ltd.	2be1e888-e0a4-7db7-e063-6294a90a77d5	2025-11-27	Warnings	Exact identifier application number: M006
EELHOE Acne	SALICYLIC ACID	Shantou Eelhoe Daily Chemical Technology Co., Ltd.	2a88a374-64bc-02a3-e063-6294a90a333e	2025-11-27	Warnings	Exact identifier application number: M006
EELHOE Mole Reduce Essence	SALICYLIC ACID	Shantou Eelhoe Daily Chemical Technology Co., Ltd.	2f80ffc4-c945-71c9-e063-6394a90add8c	2025-11-27	Warnings	Exact identifier application number: M006
JAYSUING ACNE PATCHES	SALICYLIC ACID	Shantou Jaysuing Cleaning and Environmental Protection Technology Co., Ltd.	29fb7bcc-a630-1fba-e063-6294a90a65c1	2025-11-27	Warnings	Exact identifier application number: M006
Relief	COLLOIDAL OATMEAL 1%	Era Organics, Inc.	0ad58a99-e41a-a830-e063-6294a90af9cb	2025-11-27	Warnings	Exact identifier application number: M006
Superbalm	COLLOIDAL OATMEAL 1%	Era Organics, Inc.	f5298e5e-583d-d74c-e053-2995a90affb5	2025-11-27	Warnings	Exact identifier application number: M006
OGEE CLEARGANICS TARGETED BLEMISH TREATMENT	SALICYLIC ACID ACNE MEDICATION	Ogee Inc	162831d3-7e95-62f4-e063-6394a90aef7c	2025-11-26	Warnings	Exact identifier application number: M006
EELHOE Pimple Patches	SALICYLIC ACID	Shantou Ximonth Biotechnology Co., Ltd.	ffd4972a-f9bd-44a4-9d29-cd5722696805	2025-11-26	Warnings	Exact identifier application number: M006
OUHOE PIMPLE	SALICYLIC ACID	Shantou Woodsleep Biotechnology Co., Ltd.	2a374e1c-0d21-e16c-e063-6394a90ab487	2025-11-26	Warnings	Exact identifier application number: M006

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
W9WZN9A0GM	BENZOYL PEROXIDE	94-36-0	BENZOYL PEROXIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
106309	benzoyl peroxide 5 % Topical Lotion	PSN	03799b2c-cab1-4672-9004-29e4873d022f	10
106309	benzoyl peroxide 50 MG/ML Topical Lotion	SCD	03799b2c-cab1-4672-9004-29e4873d022f	10
106309	benzoyl peroxide 5 % Topical Lotion	SY	03799b2c-cab1-4672-9004-29e4873d022f	10

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
70764-106-11	70764010611	74 mL in 1 TUBE	74 ml					Historical
70764-106-51	70764010651	1 TUBE in 1 BOX (70764-106-51) / 74 mL in 1 TUBE (70764-106-11)	1 tube	2016-06-09	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
CONTROL CORRECTIVE - CLEAR MED 5% (70764-106)	CONTROL CORRECTIVE SKINCARE INC	2025-12-31	HUMAN OTC DRUG LABEL	10