SULFUR CALMING MASK

Product NDC: 70764-103
11-digit product format: 707640103
Labeler code: 70764
Product ID: 70764-103_474bb0d3-4c59-f300-e063-6394a90a608a
Type: HUMAN OTC DRUG
Nonproprietary name: SULFUR
Dosage form: CREAM
Route: TOPICAL
Labeler: CONTROL CORRECTIVE SKINCARE INC
Application: M006
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2018-09-11
Substance: SULFUR
Active strength: 10 g/100g
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	70764-103-52	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	70764-103-52	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	70764-103-52	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	70764-103-52	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	70764-103-52	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	70764-103-52	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	70764-103-52	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	70764-103-52	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	70764-103-52	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: SULFUR CALMING MASK
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SULFUR	10 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
70FD1KFU70	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1053330	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
446bd2ea-da88-422a-b086-e61b2d5b6269	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70764-103-52	2025-12-31	C162847	48780-1	2cef2736-6a93-d83d-e063-dadaa90ab31f	CONTROL CORRECTIVE - SULFUR CALMING MASK (70764-103)
70764-103-52	2025-01-30	C162847	48780-1	2cef2736-6a93-d83d-e063-dadaa90ab31f	CONTROL CORRECTIVE - SULFUR CALMING MASK (70764-103)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70764-103-22	SULFUR CALMING MASK	57 g in 1 JAR	CREAM	57		5
70764-103-52	SULFUR CALMING MASK	1 in 1 BOX	CREAM	1		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70764-103	SULFUR CALMING MASK (SULFUR) CREAM [CONTROL CORRECTIVE SKINCARE INC]	4	Current NDC, Legacy NDC, 2 package rows	20230923_446bd2ea-da88-422a-b086-e61b2d5b6269.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 5 of 56 · 1,101 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
10% Azelaic Acid	AZELAIC ACID CREAM	Guangzhou Ariel Medical Technology Co., Ltd.	55b03daa-b6d4-9edf-e063-6394a90ac4d1	2026-07-03	Warnings	Exact identifier application number: M006
Hero Mighty Cleanser	SALICYLIC ACID	Church & Dwight Co., Inc.	5597df54-2e58-0d6a-e063-6394a90a1697	2026-07-01	Warnings	Exact identifier application number: M006
Hero Pore Cleanser	SALICYLIC ACID	Church & Dwight Co., Inc.	559987c0-7abe-13fc-e063-6294a90a9f27	2026-07-01	Warnings	Exact identifier application number: M006
Acne Treatment Cream	2% SALICYLIC ACID	Zytrell Skin Solutions Inc.	555be487-92d8-6220-e063-6394a90a0c0a	2026-06-28	Warnings	Exact identifier application number: M006
SKINTIFIC 3X ACID INTENSIVE ACNE TREATMENT	SALICYLIC ACID	Longway Technology(Guangzhou)Co., Ltd.	553957ef-cb8a-e75d-e063-6394a90a261b	2026-06-27	Warnings	Exact identifier application number: M006
ORLASKIN ACNE Treatment	SALICYLIC ACID	Guangzhou Yapheon Health Industry Co., Ltd.	552bf5df-0a3c-7c10-e063-6394a90a311f	2026-06-26	Warnings	Exact identifier application number: M006
ORLASKIN SALICYLIC ACID ACNE TREATMENT PADS	SALICYLIC ACID	Guangzhou Yapheon Health Industry Co., Ltd.	552c9e72-db4b-641a-e063-6294a90a2901	2026-06-26	Warnings	Exact identifier application number: M006
CosmoClear Cleanser	SALICYLIC ACID	Noon Aesthetics M.R. Ltd	dd738dfd-676b-40fe-8b0e-3d8305e0fdcb	2026-06-25	Warnings	Exact identifier application number: M006
Walgreens Acne Foaming Cleanser	BENZOYL PEROXIDE	WALGREEN COMPANY	549fddb8-9d42-16cb-e063-6294a90aa2a9	2026-06-19	Warnings	Exact identifier application number: M006
Walgreens Maximum Strength Acne Treatment	BENZOYL PEROXIDE	WALGREEN COMPANY	548e327b-1a4f-03df-e063-6294a90a3932	2026-06-18	Warnings	Exact identifier application number: M006
Epoch	SALICYLIC ACID	NSE Products, Inc.	3084ac37-de1f-4218-9471-6a5ebf720eb9	2026-06-17	Warnings	Exact identifier application number: M006
VICHY LABORATOIRES NORMADERM ACNE CONTROL DAILY MOISTURIZER	SALICYLIC ACID	LOreal USA Products Inc	17b7a58b-97f2-429f-83cb-db04631d307d	2026-06-16	Warnings	Exact identifier application number: M006
VICHY LABORATOIRES NORMADERM ACNE CONTROL DAILY MOISTURIZER	SALICYLIC ACID	Cosmetique Active Production	17b8a58b-97f2-429f-83cb-db04631d307d	2026-06-16	Warnings	Exact identifier application number: M006
Societe Clarity Bac	SALICYLIC ACID	Societe Clinical Skincare	545130ce-46f9-c231-e063-6394a90a1ea8	2026-06-16	Warnings	Exact identifier application number: M006
ES Salicylic Wash	SALICYLIC ACID	Elaine Sterling Enterprises	543ab052-5aa9-6585-e063-6394a90af88f	2026-06-16	Warnings	Exact identifier application number: M006
Societe Clear Skin Pads	SALICYLIC ACID	Societe Clinical Skincare	543a4347-d7d8-3050-e063-6294a90ab3a2	2026-06-16	Warnings	Exact identifier application number: M006
FHF Crisp Start	ACNE CLEANSER	Summer Soles LLC dba Farmhouse Fresh Goods	54391292-263d-253e-e063-6394a90a742f	2026-06-16	Warnings	Exact identifier application number: M006
FHF Change Peel Pads	SALICYLIC PADS	Summer Soles, LLC dba Farmhouse Fresh Goods	5439a9dd-786c-9140-e063-6394a90a8fa9	2026-06-16	Warnings	Exact identifier application number: M006
FHF Day Breakthru	SALICYLIC SERUM	Summer Doles dba Farmhouse Fresh Fresh Goods	54397bb7-1845-72a7-e063-6394a90abbd1	2026-06-16	Warnings	Exact identifier application number: M006
Societe Daily Exfoliation	SALICYLIC ACID	Societe Clinical Skincare	54633a24-3761-14d7-e063-6294a90a89f9	2026-06-16	Warnings	Exact identifier application number: M006

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
70FD1KFU70	SULFUR	7704-34-9	SULFUR

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1053330	sulfur 10 % Medicated Liquid Soap	PSN	446bd2ea-da88-422a-b086-e61b2d5b6269	5
1053330	sulfur 100 MG/ML Medicated Liquid Soap	SCD	446bd2ea-da88-422a-b086-e61b2d5b6269	5
1053330	sulfur 10 % Medicated Liquid Soap	SY	446bd2ea-da88-422a-b086-e61b2d5b6269	5
1053330	sulfur 10 % Topical Mask	SY	446bd2ea-da88-422a-b086-e61b2d5b6269	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
70764-103-22	70764010322	57 g in 1 JAR	57 g					Historical
70764-103-52	70764010352	1 JAR in 1 BOX (70764-103-52) / 57 g in 1 JAR (70764-103-22)	1 jar	2018-09-11	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
CONTROL CORRECTIVE - SULFUR CALMING MASK (70764-103)	CONTROL CORRECTIVE SKINCARE INC	2025-12-31	HUMAN OTC DRUG LABEL	5