AVEDA SCALP REMEDY DADRUFF

Product NDC
57677-065
11-digit product format
576770065
Labeler code
57677
Product ID
57677-065_ef2c4a93-864c-f147-e053-2995a90ae207
Type
HUMAN OTC DRUG
Nonproprietary name
SALICYLIC ACID
Dosage form
SOLUTION
Route
TOPICAL
Labeler
Aveda Corporation
Application
M032
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2022-12-06
Marketing end
0000-00-00
Substance
SALICYLIC ACID
Active strength
20 mg/mL
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct57677-065DDiscontinued by firm2026-10-16
excluded packagepackage57677-06557677-065-01DDiscontinued by firm2026-10-16

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 · 22 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage57677-065-01d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage57677-065-01f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31excluded productproduct2ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-31excluded packagepackage57677-065-012ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28excluded productproducta1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-28excluded packagepackage57677-065-01a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21excluded productproductcfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-21excluded packagepackage57677-065-01cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10excluded productproductcdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-10excluded packagepackage57677-065-01cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31excluded productproduct302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-31excluded packagepackage57677-065-01302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20excluded productproducted331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-20excluded packagepackage57677-065-01ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10excluded productproduct0efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-10excluded packagepackage57677-065-010efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08excluded productproductad56d346431e…cc804d4bbf1e…
2024-11-09 02:27 UTC · source 2024-11-08excluded packagepackage57677-065-01ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03excluded productproduct367a005e9d99…383a685ebd0f…
2024-10-04 04:10 UTC · source 2024-10-03excluded packagepackage57677-065-01367a005e9d99…383a685ebd0f…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57677-065-012023-11-03C16284748780-10191ceaa-69a2-198a-e063-dbdaa90aec3eef2c4a93-864b-f147-e053-2995a90ae207
57677-065-012023-07-28C16284748780-10191ceaa-69a2-198a-e063-dbdaa90aec3eef2c4a93-864b-f147-e053-2995a90ae207

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 10 of 31 · 615 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Dry ScalpPYRITHIONE ZINCValu Merchandisers Company6349fd91-675b-4489-8b57-e584f718ca3f2026-02-16Warnings, Adverse reactionsExact identifier
application number: M032
Dry Scalp CarePYRITHIONE ZINCValu Merchandisers Companye9fc676c-0313-430f-a422-6dba51241bd52026-02-16Warnings, Adverse reactionsExact identifier
application number: M032
DandruffPYRITHIONE ZINCValu Merchandisers Companyd5dd333d-fea5-4e03-bd9f-cbc28ea48a802026-02-16Warnings, Adverse reactionsExact identifier
application number: M032
DandruffPYRITHIONE ZINCUnited Natural Foods, Inc. dba UNFI66f301bf-8e2e-43ce-b6b8-0983fe795f012026-02-16Warnings, Adverse reactionsExact identifier
application number: M032
Tuymec Anti-Dandruff Shampoo.ANTI-DANDRUFF SHAMPOO.Guangzhou Jingliang Cosmetics Co., Ltd.4ae93408-5c8f-c0a5-e063-6394a90a9e0d2026-02-15WarningsExact identifier
application number: M032
RoyceDerm Seborrheic Dermatitis and Psoriasis Treatment creamSALICYLIC ACID 3%RoyceDerm LLC4ac42528-9210-6936-e063-6294a90a41682026-02-14WarningsExact identifier
application number: M032
OLIVITA 5% Minoxidil5% MINOXIDILShenzhen Xinxin Yunhai Technology Co., Ltd.4acbdf3d-976a-2cba-e063-6294a90a35e62026-02-14WarningsExact identifier
application number: M032
VENANOCI MinoxidilMINOXIDILShenzhen Xinxin Yunhai Technology Co., Ltd.4acc38aa-13da-981b-e063-6294a90aede52026-02-14WarningsExact identifier
application number: M032
Everyday Clean DandruffPYRITHIONE ZINCTopco Associates LLCfc568c8f-0d59-4b26-8f72-ea70e43166872026-02-13Warnings, Adverse reactionsExact identifier
application number: M032
DandruffPYRITHIONE ZINCTopco Associates LLCa0f2c58b-bb17-42a3-bd90-be771f60ef202026-02-13Warnings, Adverse reactionsExact identifier
application number: M032
DandruffPYRITHIONE ZINCTopco Associates LLC706b856c-ce89-4860-bc5d-9803deb469e72026-02-13Warnings, Adverse reactionsExact identifier
application number: M032
Dry Scalp CarePYRITHIONE ZINCTopco Associates LLC3300bfd5-ae84-4bc8-a4cd-05472b498fb72026-02-13Warnings, Adverse reactionsExact identifier
application number: M032
Everyday CleanPYRITHIONE ZINCTopco Associates LLCc0abb41f-9df0-4493-8452-592ec30c79242026-02-13Warnings, Adverse reactionsExact identifier
application number: M032
2 in 1 DandruffPYRITHIONE ZINCTopco Associates LLC7da1e057-a69e-4b89-a309-919d88da3b932026-02-13Warnings, Adverse reactionsExact identifier
application number: M032
Pyrithione zincPYRITHIONE ZINCTopco Associates LLC2c1420a8-404f-4fd7-8f07-cd441b390ac22026-02-13Warnings, Adverse reactionsExact identifier
application number: M032
Everyday Clean DandruffPYRITHIONE ZINCWinCo Foods, LLC2581c531-c068-4dae-b569-3b1f86dad0662026-02-12Warnings, Adverse reactionsExact identifier
application number: M032
Dry ScalpPYRITHIONE ZINCWinCo Foods, LLC4fca1200-dc6c-4e6e-b09c-2ec8ac0fa4112026-02-12Warnings, Adverse reactionsExact identifier
application number: M032
Everyday Clean 2 in 1PYRITHIONE ZINCWinCo Foods, LLC8bd391ae-0eeb-4e7d-b1e5-20e4adb1da172026-02-12Warnings, Adverse reactionsExact identifier
application number: M032
Everyday Clean 2 in 1PYRITHIONE ZINCYour Military Exchangesa62b282f-e928-42bb-b595-d5f2066aac632026-02-12Warnings, Adverse reactionsExact identifier
application number: M032
natouchPYRITHIONE ZINCNatouch LLC0f330e2d-25d7-5e0e-e063-6394a90acda92026-02-10WarningsExact identifier
application number: M032

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
57677-065-0157677006501125 mL in 1 BOTTLE, SPRAY (57677-065-01) 125 ml2022-12-060000-00-00NoNoCurrent