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 17 of 31 · 615 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
DermaZinc	PYRITHIONE ZINC	WynnPharm Inc	e73010ae-291d-6adf-e053-2a95a90a8aea	2025-11-14	Warnings	Exact identifier application number: M032
Head and Shoulders 2in1 Men Advanced Series Pure Sport Old Spice	PYRITHIONE ZINC	The Procter & Gamble Manufacturing Company	7bbd2559-4aba-9f18-e053-2991aa0a152e	2025-11-13	Warnings	Exact identifier application number: M032
Divine Dandrene 1%	ZINC PYRITHIONE	DS Healthcare Group, Inc.	ab605699-4090-45a3-882f-44379fe2a82e	2025-11-11	Warnings	Exact identifier application number: M032
Divine Dandrene 2%	ZINC PYRITHIONE	DS Healthcare Group, Inc.	54b0a610-dd15-4064-9feb-4d30b5e522ad	2025-11-11	Warnings	Exact identifier application number: M032
Dandrene Anti-Dandruff Conditioner	ZINC PYRITHIONE	DS Healthcare Group, Inc.	aed49bfe-e016-46ac-a025-81b47cc08147	2025-11-11	Warnings	Exact identifier application number: M032
Minoxidil hair growth serum	MINOXIDIL HAIR GROWTH SERUM	Jiashen International Trade Limited	26cc22be-30f6-03da-e063-6394a90aafe7	2025-11-09	Warnings	Exact identifier application number: M032
Sulfur 8 Kids Anti-Dandruff	PYRITHIONE ZINC	J. Strickland & Co.	89f4ecc8-7a49-42cb-b85d-71c9299e6712	2025-11-07	Warnings	Exact identifier application number: M032
Sulfur 8 Aqua Blue	PYRITHIONE ZINC	J. Strickland & Co.	cdcf3cea-4a5d-4b8b-b47d-3163f9837d16	2025-11-07	Warnings	Exact identifier application number: M032
Sulfur 8 Scalp Therapy Medicated Dandruff Control	PYRITHIONE ZINC	J. Strickland and Co.	96b26da0-d0d7-77ed-e053-2995a90a7a78	2025-11-07	Warnings	Exact identifier application number: M032
Shailee Psoriasis Treatment	SALICYLIC ACID	Foshan Sugar Max Cosmetics CO.,Ltd	02a71ce4-baf5-4231-afd6-21ef0b22e931	2025-11-05	Warnings	Exact identifier application number: M032
Sulfur 8 Kids Anti-Dandruff Hair and Scalp Conditioner	SULFUR	J. Strickland & Co.	8e9da3fd-701e-4354-bb00-ecd4dab48fa3	2025-11-03	Warnings	Exact identifier application number: M032
Denorex Severe Flakes Medicated Anti Dandruff	PYRITHIONE ZINC	Neoteric Cosmetics, Inc.	41ad0d3a-0704-44c9-e063-6394a90ad40d	2025-10-21	Warnings	Exact identifier application number: M032
Stay Minoxidil Hair Regrowth Treatment	MINOXIDIL 5%	HALORIA INC.	41b745d7-6947-ec24-e063-6294a90aa467	2025-10-21	Warnings	Exact identifier application number: M032
DERMOSCRIBE SEBORRHEIC DERMATITIS	SULFUR, SALICYLIC ACID, HYDROCORTISONE	DERMOSCRIBE PTY LTD	2b6bf90b-5d42-4c08-afee-56e13122285e	2025-10-17	Warnings	Exact identifier application number: M032
Shea Moisture	APPLE CIDER VINEGAR INSTANT SCALP REFRESH ANTI-DANDRUFF SPRAY	Conopco, Inc. d/b/a Unilever	414ab8ec-165c-21f8-e063-6294a90adc4f	2025-10-16	Warnings	Exact identifier application number: M032
Shea Moisture	APPLE CIDER VINEGAR ANTI-DANDRUFF LEAVE-IN	Conopco, Inc. d/b/a Unilever	414b7fd2-6a65-af39-e063-6394a90a00b8	2025-10-16	Warnings	Exact identifier application number: M032
Seacall Natural Cedarwood Oil	NATURAL CEDARWOOD OIL	Guangdong Quadrant Ecological Technology Co., Ltd.	1f4ebe4d-6e93-378c-e063-6394a90aec95	2025-10-15	Warnings	Exact identifier application number: M032
RemedyDandruffShampooTreatment	ACTIIV REMEDY DANDRUFF SHAMPOO TREATMENT	Naturich Cosmetique Labs	129fd043-6643-cc46-e063-6294a90a6eae	2025-10-08	Warnings	Exact identifier application number: M032
Head and Shoulders Clinical Strength Cooling Itch Relief	SELENIUM SULFIDE	The Procter & Gamble Manufacturing Company	40464e2d-f738-33ec-e063-6394a90a02c2	2025-10-03	Warnings	Exact identifier application number: M032
Head and Shoulders 2in1 Clinical Strength Cooling Itch Relief	SELENIUM SULFIDE	The Procter & Gamble Manufacturing Company	4046c345-e1ac-0ecc-e063-6294a90a59fa	2025-10-03	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