NDC 81817-101-01 - ZENOTRI Scalp Essence
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
- 81817-101
- Requested NDC
- 81817-101-01
- Package NDCs from labels
- 81817-101-01, 81817-101-03, 81817-101-02
- Manufacturer
- CHROMACH Co., Ltd. | SUANN HYANGJANG Co.,LTD
- Effective date
- 2021-05-13
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ZENOTRI Scalp Essence - CHROMACH Co., Ltd. | SUANN HYANGJANG Co.,LTD | CHROMACH Co., Ltd. | SUANN HYANGJANG Co.,LTD | 2021-05-13 | HUMAN OTC DRUG LABEL |
| ZENOTRI Scalp Essence - CHROMACH Co., Ltd. | SUANN HYANGJANG Co.,LTD | CHROMACH Co., Ltd. | SUANN HYANGJANG Co.,LTD | 2021-04-22 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 81817-101-03 | 2023-01-30 | C162847 | 48780-1 | f386c64a-2ff5-0266-e053-dadaa90a7c1a | c231cbcd-4fe5-16ba-e053-2a95a90a2f8d |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 81817-101-01 | ZENOTRI Scalp Essence | 25 mL in 1 TUBE | GEL | 25 | 3 | |
| 81817-101-03 | ZENOTRI Scalp Essence | 1 in 1 CARTON | GEL | 1 | 3 |
DailyMed Dashboard NDC Coverage#
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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| Salicylic acid | CALLUS REMOVERS | Premier Brands of America Inc. | 0b637f58-5604-454d-99ba-24115113ac3d | 2026-05-18 | Warnings | O414PZ4LPZ |
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| Pain Relief Gel-Patch | LIDOCAINE AND MENTHOL | Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. | 0ae6cfd1-bbea-3fe6-e063-6294a90a541f | 2026-05-17 | Warnings | L7T10EIP3A |
| Menthol Pain Relief Gel-Patch | MENTHOL | Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. | 0ae7af3a-7dfc-9736-e063-6394a90abe3c | 2026-05-17 | Warnings | L7T10EIP3A |
| Pain Relief Gel-Patch | LIDOCAINE AND MENTHOL | Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. | 32e1df3a-2f8f-68df-e063-6294a90aa1d1 | 2026-05-17 | Warnings | L7T10EIP3A |
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| CounterAct Cough Drops Orchard Cherry | MENTHOL | Melaleuca, Inc. | 6049842c-d763-4a91-a225-976ed74e1693 | 2026-05-15 | Warnings | L7T10EIP3A |
| CounterAct Cough Drops Honey Lemon | MENTHOL | Melaleuca, Inc. | 84ac3489-9d64-401f-ab78-715af4de5440 | 2026-05-15 | Warnings | L7T10EIP3A |
| Biofreeze Overnight Gel | MENTHOL | Reckitt Benckiser LLC | f5c8c08b-c7c0-f84d-e053-2a95a90add15 | 2026-05-15 | Warnings | L7T10EIP3A |
| Biofreeze Professional | MENTHOL, UNSPECIFIED FORM | Reckitt Benckiser LLC | 00bba5d2-b0e0-701c-e063-6294a90a5741 | 2026-05-15 | Warnings | L7T10EIP3A |
| Biofreeze Overnight Roll-on | MENTHOL | Reckitt Benckiser LLC | f67d7b7a-8922-73f6-e053-2995a90a2e80 | 2026-05-15 | Warnings | L7T10EIP3A |
| Biofreeze Overnight Relief | MENTHOL, UNSPECIFIED FORM | Reckitt Benckiser LLC | 07be6e88-1850-4d6a-946d-f03830b8c4a2 | 2026-05-15 | Warnings | L7T10EIP3A |
| Biofreeze Professional | MENTHOL, UNSPECIFIED FORM | Reckitt Benckiser LLC | 6bef9ccb-7a5a-4c67-b1bc-a92b167312da | 2026-05-15 | Warnings | L7T10EIP3A |
| Biofreeze Roll-On | MENTHOL | Reckitt Benckiser LLC | ebbbe9cb-b1ce-4dac-9fca-f54a2470c4fb | 2026-05-15 | Warnings | L7T10EIP3A |
| Biofreeze Precision Relief Pen | MENTHOL | Reckitt Benckiser LLC | b4cc1db5-a33f-17bc-e053-2995a90ab7eb | 2026-05-15 | Warnings | L7T10EIP3A |
| Biofreeze Professional | MENTHOL, UNSPECIFIED FORM | Reckitt Benckiser LLC | db982baf-31ea-4f09-90e3-cd5facb5dfe5 | 2026-05-15 | Warnings | L7T10EIP3A |
| Biofreeze Professional Roll-On | MENTHOL, UNSPECIFIED FORM | Reckitt Benckiser LLC | f62f8ec3-593d-480a-85a0-01fcd7f1790c | 2026-05-15 | Warnings | L7T10EIP3A |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.