Home NDC 57677-065-01 AVEDA SCALP REMEDY DADRUFF
Product NDC 57677-065
Requested package NDC 57677-065-01
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 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 · 11 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# 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 28 of 31 · 613 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join XtraCare Anti-Dandruff Hair Cleanse Coconut and Shea Butter PYRITHIONE ZINC Rejoice International Inc. 7d9bf611-db24-4915-9b13-b7b36f47711f 2024-02-28 Warnings Exact identifier application number: M032 XtraCare Anti-Dandruff Hair Cleanse mint and eucalyptus PYRITHIONE ZINC Rejoice International Inc. b05742fe-692f-45a3-9de0-5f3f08642d78 2024-02-28 Warnings Exact identifier application number: M032 XtraCare Dandruff Hair Wash SALICYLIC ACID Rejoice International 1902e6bb-e829-4b1a-b85a-1394913c77ca 2024-02-28 Warnings Exact identifier application number: M032 amazon basics maximum strength dandruff Anti-dandruff SELENIUM SULFIDE AMAZON.COM SERVICES LLC 194e4c51-ff7b-4def-a71d-efa5dfca3efd 2024-02-26 Warnings Exact identifier application number: M032 Doo Gro Braids Twists Locs Dandruff Control Moisturizing SALICYLIC ACID J. Strickland and Co. 116f4f0d-66c7-49dd-e063-6394a90ab2b5 2024-02-15 Warnings Exact identifier application number: M032 amazon basics therapeutic tar anti-dandruff Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis COAL TAR AMAZON.COM SERVICES LLC ada1be0c-53a7-443c-bc3c-f7a26b5f96a9 2024-02-05 Warnings Exact identifier application number: M032 Equate Dry Scalp 2 in 1 Dandruff Anti-Dandruff PYRITHIONE ZINC Wal-Mart Stores, Inc. 6440fdd9-daa8-4f15-bdee-33724993bd7b 2024-02-01 Warnings Exact identifier application number: M032 Equate Everyday Clean Dandruff Anti-Dandruff PYRITHIONE ZINC Wal-Mart Stores, Inc. 4c84a67a-1f43-4f40-a172-271de7e76785 2024-01-29 Warnings Exact identifier application number: M032 Equate Everyday Clean 2 in 1 Dandruff Anti-Dandruff PYRITHIONE ZINC Wal-Mart Stores, Inc. c85095f2-5dbd-4822-a83a-dc3641c4a330 2024-01-29 Warnings Exact identifier application number: M032 Hydrocortisone ANTIPRURITIC (ANTI-ITCH) Dynarex Corporation 81dff9df-6f7e-49f0-e053-2a91aa0af7e7 2024-01-23 Warnings Exact identifier application number: M032 Walgreens Original T-Gel Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis COAL TAR Walgreen Company 42cc63ab-6f79-4544-8529-7b8c36021b18 2024-01-22 Warnings Exact identifier application number: M032 True plus Real Therapeutic T plus Plus Original Strength Tar Dandruff Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis COAL TAR Garcoa, Inc. 1f4c23d5-ca00-4387-abc7-59d9ef471977 2024-01-22 Warnings Exact identifier application number: M032 Walgreens Extra Strength T-Gel Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis COAL TAR Walgreen Company 7f681386-976c-40f4-8b18-97413989ab78 2024-01-22 Warnings Exact identifier application number: M032 Prosoria Medicated SELENIUM SULFIDE Nuvothera, Inc. 44eaaeb0-1400-4697-85d0-e8c2282c1cba 2024-01-11 Warnings Exact identifier application number: M032 Prosoria Scalp SALICYLIC ACID Nuvothera, Inc. 52a98715-3e57-4b86-b91e-0ce433dc22bd 2024-01-10 Warnings Exact identifier application number: M032 Prosoria Psoriasis Treatment SALICYLIC ACID Nuvothera, Inc. f94f4481-c58e-4555-9863-cbaa2c4cdd07 2024-01-10 Warnings Exact identifier application number: M032 Equate Therapeutic Dandruff Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis COAL TAR Wal-Mart Stores, Inc. 408d57e4-a707-4826-a04c-99517dc9b5af 2024-01-04 Warnings Exact identifier application number: M032 Equate Extra Strength Therapeutic Dandruff Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis COAL TAR Wal-Mart Stores, Inc. 986ac1ab-c7c3-40df-b41b-6f26cce22a43 2024-01-04 Warnings Exact identifier application number: M032 Pert Plus 2 in 1 Anti-Dandruff PYRITHIONE ZINC TCP HRB Holdings ecfa3d29-b54c-265c-e053-2995a90a8020 2024-01-01 Warnings Exact identifier application number: M032 CeraVe Developed with Dermatologists Psoriasis Moisturizing SALICYLIC ACID L'Oreal USA Products Inc 51f27970-92d3-44ae-b2b1-d820719680fe 2023-12-28 Warnings Exact identifier application number: M032
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 57677-065-01 57677006501 125 mL in 1 BOTTLE, SPRAY (57677-065-01) 125 ml 2022-12-06 0000-00-00 No No Current