NDC 57677-005-01 - Aveda Active Composition
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 57677-005
- Requested NDC
- 57677-005-01
- Package NDCs from labels
- 57677-005-01, 57677-005-02
- Manufacturer
- Aveda Corporation | Les Emballages Knowlton Inc.
- Effective date
- 2011-03-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| AVEDA ACTIVE COMPOSITION | Aveda Corporation | Les Emballages Knowlton Inc. | 2011-03-08 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 57677-005-02 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-afcc-f424-e053-dadaa90a57ce | AVEDA ACTIVE COMPOSITION |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 57677-005-01 | Aveda Active Composition | 50 mL in 1 BOTTLE, GLASS | LIQUID | 50 | 1 | |
| 57677-005-02 | Aveda Active Composition | 1 in 1 BOX | LIQUID | 1 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
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.
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| Camphor 4% Plus Menthol 10% | CAMPHOR 4% PLUS MENTHOL 10% | PureTek Corporation | 3cab26e4-e377-f26a-e063-6394a90a17af | 2025-08-20 | Warnings | L7T10EIP3A |
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| Game On | MENTHOL, METHYL SALICYLATE | Natural Essentials, Inc. | 3cd20f1f-033f-f698-e063-6294a90a89eb | 2025-08-20 | Warnings | L7T10EIP3A LAV5U5022Y |
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| METHYL SALICYLATE 25% | METHYL SALICYLATE | Oncora Pharma, LLC | 3c4bc55d-6582-3b5e-e063-6394a90a994c | 2025-08-13 | Warnings | LAV5U5022Y |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.