PowerSpot Cleanse

Product NDC: 72203-014
11-digit product format: 722030014
Labeler code: 72203
Product ID: 72203-014_458a8017-d202-e4ec-e063-6294a90a0103
Type: HUMAN OTC DRUG
Nonproprietary name: Sulfur
Dosage form: SOAP
Route: TOPICAL
Labeler: Bluemercury
Application: M006
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2019-03-15
Substance: SULFUR
Active strength: 30 mg/mL
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 · 24 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	72203-014-01	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	72203-014-02	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	72203-014-01	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	72203-014-02	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	72203-014-01	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	72203-014-02	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	72203-014-01	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	72203-014-02	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	72203-014-01	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	72203-014-02	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	72203-014-01	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	72203-014-02	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	72203-014-01	`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	72203-014-02	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	72203-014-01	`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	72203-014-02	`1332a3947898…`	`d4bfe170f9cd…`

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: PowerSpot Cleanse
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SULFUR	30 mg/mL

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
1046894	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
443ae172-bacd-4122-8d78-d2214bcb02fd	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277	Product name	1	20190408

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
72203-014-01	2025-01-29	PowerSpot Cleanse
72203-014-02	2025-01-29	PowerSpot Cleanse
72203-014-01	2024-01-30	PowerSpot Cleanse
72203-014-02	2024-01-30	PowerSpot Cleanse

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
72203-014-01	PowerSpot Cleanse	1 in 1 CARTON	SOAP	1	4
72203-014-01	PowerSpot Cleanse	120 mL in 1 TUBE	SOAP	120	4
72203-014-02	PowerSpot Cleanse	1 in 1 CARTON	SOAP	1	4
72203-014-02	PowerSpot Cleanse	50 mL in 1 TUBE	SOAP	50	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72203-014	POWERSPOT CLEANSE (SULFUR) SOAP [BLUEMERCURY]	3	Current NDC, Legacy NDC, 4 package rows	20250130_443ae172-bacd-4122-8d78-d2214bcb02fd.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 55 of 55 · 1,088 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Replenix Acne Gly-Sal 2-2 Foaming Cleanser	SALICYLIC ACID	Topiderm, Inc.	811dbf95-2b39-45c5-99a2-33c3c9d19570	2019-12-19	Warnings	Exact identifier application number: M006
REPLENIX ACNE SOLUTIONS WASH	BENZOYL PEROXIDE	Topiderm, Inc.	8dc2d27d-3cc4-4874-b4c2-32607849b205	2019-12-17	Warnings	Exact identifier application number: M006
REPLENIX ACNE Solution BENZOYL PEROXIDE WASH	BENZOYL PEROXIDE	Topiderm, Inc.	235e9dd5-13f2-4078-9807-1d87fd9e6cba	2019-12-17	Warnings	Exact identifier application number: M006
Replenix Acne	BENZOYL PEROXIDE	Topiderm, Inc	03d4c298-8f44-41f7-b086-96ae836152bb	2019-10-31	Warnings	Exact identifier application number: M006
Replenix Acne	BENZOYL PEROXIDE	Topiderm, Inc.	c12f9005-a549-4447-9beb-df7126f77df1	2019-10-31	Warnings	Exact identifier application number: M006
Gly-Sal 10-2 Pads	SALICYLIC ACID	Topiderm, Inc.	b39e845d-4c40-4f9e-9cb5-a8386f326652	2019-10-23	Warnings	Exact identifier application number: M006
Gly-Sal 5-2 Pads	SALICYLIC ACID	Topiderm, Inc.	e73bd26c-cdc2-47ab-94e8-3bc49a9b19e8	2019-10-22	Warnings	Exact identifier application number: M006
SKIN MEDICA Purifying Foaming Wash	SALICYLIC ACID	Allergan, Inc.	064d9e2b-077f-4229-b653-666fc5479ae2	2013-03-01	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
1046894	sulfur 3 % Medicated Liquid Soap	PSN	443ae172-bacd-4122-8d78-d2214bcb02fd	4
1046894	sulfur 30 MG/ML Medicated Liquid Soap	SCD	443ae172-bacd-4122-8d78-d2214bcb02fd	4
1046894	sulfur 3 % Medicated Liquid Soap	SY	443ae172-bacd-4122-8d78-d2214bcb02fd	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
72203-014-01	72203001401	1 TUBE in 1 CARTON (72203-014-01) / 120 mL in 1 TUBE	1 tube	2019-03-15	0000-00-00	No	No	Current
72203-014-02	72203001402	1 TUBE in 1 CARTON (72203-014-02) / 50 mL in 1 TUBE	1 tube	2019-03-15	0000-00-00	No	No	Current