NATUREPLEX PSORIASIS

Product NDC: 67234-073
11-digit product format: 672340073
Labeler code: 67234
Product ID: 67234-073_31269712-42a5-44bd-8f6f-196f934d75c4
Type: HUMAN OTC DRUG
Nonproprietary name: SALICYLIC ACID
Dosage form: CREAM
Route: TOPICAL
Labeler: Natureplex, LLC
Application: M032
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2019-07-24
Substance: SALICYLIC ACID
Active strength: 20 mg/g
NDC exclude flag: No
Listing certified through: 2027-12-31
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	67234-073-01	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	67234-073-01	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	67234-073-01	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	67234-073-01	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	67234-073-01	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	67234-073-01	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	67234-073-01	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	67234-073-01	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	67234-073-01	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: NATUREPLEX PSORIASIS
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SALICYLIC ACID	20 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
O414PZ4LPZ	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
317152	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
1efa3e8d-f80b-44f4-a233-187e3329dd8f	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
60c52429-fcef-eb54-2387-43bc9e4f296b	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
67234-073-01	2025-01-30	C162847	48780-1	2cef2736-9819-d83d-e063-dadaa90ab31f	NATUREPLEX™ PSORIASIS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
67234-073-01	NATUREPLEX PSORIASIS	28 g in 1 TUBE	CREAM	28		3
67234-073-01	NATUREPLEX PSORIASIS	1 in 1 CARTON	CREAM	1		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
67234-073	NATUREPLEX PSORIASIS (SALICYLIC ACID) CREAM [NATUREPLEX LLC]	2	Current NDC, Legacy NDC, 2 package rows	20210114_1efa3e8d-f80b-44f4-a233-187e3329dd8f.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 8 of 31 · 615 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
2 in 1 Dandruff	PYRITHIONE ZINC	Old East Main Co.	1d4966d1-02d9-4b70-acc2-88a8190f920c	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M032
Pyrithione zinc	PYRITHIONE ZINC	Old East Main Co.	f17154e2-1bcf-43f9-b201-e84d374a0591	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M032
2 in 1 Dandruff	PYRITHIONE ZINC	Old East Main Co.	61bf3788-b1e8-4d7e-ac56-cf209ba39085	2026-03-02	Warnings, Adverse reactions	Exact identifier application number: M032
Everyday Clean Dandruff	PYRITHIONE ZINC	The Kroger Co.	835270e7-ba6a-46e8-a617-f5df1c69d411	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M032
Dry Scalp Care	PYRITHIONE ZINC	The Kroger Co.	837d7a14-b312-4dce-a00a-623b50329378	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M032
Everyday Clean	PYRITHIONE ZINC	The Kroger Co.	d442e1af-e31a-4de6-b358-52e08aedd7ee	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M032
Clean Apple	PYRITHIONE ZINC	The Kroger Co.	00eb0594-cfa5-4fdb-aca8-650c10997924	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M032
Dandruff	PYRITHIONE ZINC	Walmart Inc.	e4fd5d8b-a916-41c3-b05e-a32dd528f00f	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M032
Dry Scalp	PYRITHIONS ZINC	Walmart Inc.	23ad86c0-5a75-4f52-8561-483708d415d6	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M032
Everyday Clean 2 in 1	PYRITHIONE ZINC	Walmart Inc.	2bafcad7-1bb7-168e-e063-6394a90a0b9e	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M032
Paul Mitchell Dandruff	ZINC PYRITHIONE	John Paul Mitchell Systems	4bc02aa8-86b1-985e-e063-6294a90aa267	2026-02-26	Warnings	Exact identifier application number: M032
Dandruff	PYRITHIONE ZINC	H E B	bdf0b3da-db37-4996-b5e5-23cf824d1d1f	2026-02-24	Warnings, Adverse reactions	Exact identifier application number: M032
Dandruff	PYRITHIONE ZINC	H E B	0927361e-a210-4e44-bbe7-fb68b240cf4f	2026-02-24	Warnings, Adverse reactions	Exact identifier application number: M032
Dry Scalp Care	PYRITHIONE ZINC	H E B	0410f6a6-6602-44fb-b223-586439938e19	2026-02-24	Warnings, Adverse reactions	Exact identifier application number: M032
Dry Scalp Dandruff	PYRITHIONE ZINC	H E B	626933cb-9c84-4f37-943c-2a9bd21fcea5	2026-02-24	Warnings, Adverse reactions	Exact identifier application number: M032
2 in 1 Dandruff	PYRITHIONE ZINC	H E B	75342eff-6bff-4fed-bd12-381edd2df681	2026-02-24	Warnings, Adverse reactions	Exact identifier application number: M032
Dandruff	SELENIUM SULFIDE	H E B	182ca790-0713-412a-9111-c0cf40f20d02	2026-02-24	Warnings, Adverse reactions	Exact identifier application number: M032
Dandruff	PYRITHIONE ZINC	Better Living Brands, LLC	03799050-cb2e-4c96-b177-55e6fc145d6b	2026-02-23	Warnings, Adverse reactions	Exact identifier application number: M032
Everyday Clean	PYRITHIONE ZINC	Perrigo Direct, Inc	c36e18cf-eec0-4972-b3b5-fe3865a438d8	2026-02-19	Warnings, Adverse reactions	Exact identifier application number: M032
Everyday Clean Dandruff	PYRITHIONE ZINC	Meijer, Inc.	34b80460-fcb9-42a8-b120-1558dc5093fa	2026-02-19	Warnings, Adverse reactions	Exact identifier application number: M032

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
O414PZ4LPZ	SALICYLIC ACID	69-72-7	SALICYLIC ACID

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
317152	salicylic acid 2 % Topical Cream	PSN	1efa3e8d-f80b-44f4-a233-187e3329dd8f	3
317152	salicylic acid 20 MG/ML Topical Cream	SCD	1efa3e8d-f80b-44f4-a233-187e3329dd8f	3
317152	salicylic acid 2 % Topical Cream	SY	1efa3e8d-f80b-44f4-a233-187e3329dd8f	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
67234-073-01	67234007301	1 TUBE in 1 CARTON (67234-073-01) / 28 g in 1 TUBE	1 tube	2019-07-24	0000-00-00	No	No	Current