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 11 of 31 · 615 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Everyday Clean Dandruff	PYRITHIONE ZINC	Retail Business Services, LLC	8fb44204-b763-4aa5-a6db-94d1b4d98b65	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M032
Dandruff	PYRITHIONE ZINC	Retail Business Services, LLC	c1d8c237-1ca8-4fdb-ba94-787d3a9e6111	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M032
Dry Scalp Dandruff	PYRITHIONE ZINC	Retail Business Services, LLC	592ec7c5-44b8-405b-88a2-f02aa6c620f0	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M032
Dry Scalp Care	PYRITHIONE ZINC	Retail Business Services, LLC	37357176-913d-4dd7-a565-ad21d4ad60a8	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M032
Dandruff	PYRITHIONE ZINC	Retail Business Services, LLC	c8c82495-f09a-4ec1-9036-e464845e02f9	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M032
2 in 1 Dandruff	PYRITHIONE ZINC	Retail Business Services, LLC	ec9d36ae-cf4e-4841-a13e-5cb0fe64c4fa	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M032
2 in 1 Dandruff	PYRITHIONE ZINC	Retail Business Services, LLC	841429c3-e15c-41cc-9ca8-6b5a21a21587	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M032
Dandruff	PYRITHIONE ZINC	Publix Super Markets, Inc.	56c2b8c2-69ea-4343-ae69-43f5966261c2	2026-02-05	Warnings, Adverse reactions	Exact identifier application number: M032
Dandruff	PYRITHIONE ZINC	Publix Super Markets, Inc.	8a204a2c-6dcb-4fc4-b265-9b95da204236	2026-02-05	Warnings, Adverse reactions	Exact identifier application number: M032
Everyday Clean Dandruff	PYRITHIONE ZINC	Harris Teeter	8594a944-a67e-4dbe-8d31-7099410ff484	2026-02-04	Warnings, Adverse reactions	Exact identifier application number: M032
Everyday Clean Dandruff	PYRITHIONE ZINC	Amazon.Com Services LLC	e30896df-e4b2-4b1f-a226-a26055a4a121	2026-02-03	Warnings, Adverse reactions	Exact identifier application number: M032
Oribe Serene Scalp Anti Dandruff	ORIBE SERENE SCALP ANTI DANDRUFF	Oribe Hair Care LLC	34c4abb5-6f96-4866-a37f-4f9be6c43f2b	2026-01-30	Warnings	Exact identifier application number: M032
NATUREPLEX PSORIASIS	SALICYLIC ACID	Natureplex, LLC	1efa3e8d-f80b-44f4-a233-187e3329dd8f	2026-01-29	Warnings	Exact identifier application number: M032 ndc (product): 67234-073
Head and Shoulders Charcoal Daily	PYRITHIONE ZINC	The Procter & Gamble Manufacturing Company	69abc8fa-eee5-d36f-e053-2991aa0a940b	2026-01-28	Warnings	Exact identifier application number: M032
WeCare Anti-Dandruff	ANTIDANDRUFF SHAMPOO	Dynarex Corporation	7fad58a3-5537-f87a-e053-2991aa0a7cdb	2026-01-28	Warnings	Exact identifier application number: M032
TriDerma Psoriasis Control Face and Body Cream	SALICYLIC ACID	Genuine Virgin Aloe Corporation	66eeaf72-1fb4-4df0-9198-41f1143c67b3	2026-01-27	Warnings	Exact identifier application number: M032
TRIDERMA Psoriasis Control	SALICYLIC ACID	Genuine Virgin Aloe Corporation	16ba7145-0e8c-48b8-b557-43ac1be317ac	2026-01-27	Warnings	Exact identifier application number: M032
DHS tar gel	COAL TAR	Person and Covey	e17bd664-748b-417c-a247-9acc7bc7eec3	2026-01-23	Warnings	Exact identifier application number: M032
Therapeutic TPlus Salicylic Acid Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis	SALICYLIC ACID	Garcoa, Inc.	620617e3-0ee1-469a-ad2b-0dda957627cc	2026-01-21	Warnings	Exact identifier application number: M032
Aloe Coal 02 Conditioner	PYRITHIONE ZINC	T. SPRUILL, LLC	e8e1fbe8-7de3-4a8e-bace-b7b2e4db1828	2026-01-19	Warnings	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