NDC 69716-210-01 - NoTS Lavender Relax Daily Mask
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
- 69716-210
- Requested NDC
- 69716-210-01
- Package NDCs from labels
- 69716-210-01, 69716-210-02
- Manufacturer
- NoTS Co.,Ltd
- Effective date
- 2016-08-17
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| NoTS Lavender Relax Daily Mask - NoTS Co.,Ltd | NoTS Co.,Ltd | 2016-08-17 | HUMAN OTC DRUG LABEL |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Medicated Multipurpose Wipes | WITCH HAZEL | QUEST USA CORP. | 0f28d5f9-b20a-ac6f-e063-6394a90ac208 | 2025-12-05 | Warnings | 101I4J0U34 |
| BUDDATE REGES INTENSIVE TREATMENT | BUTYLENE GLYCOL, HYDROGENATED COCONUT OIL, BUTYROSPERMUM PARKII (SHEA) BUTTER, PALMITOYL TRIPEPTIDE-1, PALMITOYL TETRAPEPTIDE-7 | BUDDATE Co Ltd | 46495321-fb14-3479-e054-00144ff88e88 | 2025-11-30 | Warnings | 3XUS85K0RA |
| BUDDATE INONOTUS OBLIQUUS WATER BRILLIANCE MASK | BUTYLENE GLYCOL, GLYCERIN, INONOTUS OBLIQUUS (MUSHROOM) EXTRACT | BUDDATE Co Ltd | 464988ad-557e-13f5-e054-00144ff8d46c | 2025-11-30 | Warnings | 3XUS85K0RA |
| XIMONTH Quick Essence | SALICYLIC ACID | Shantou Ximonth Biotechnology Co., Ltd. | 4256f607-c9cf-cd0f-e063-6394a90a5487 | 2025-11-26 | Warnings | 101I4J0U34 |
| Meicated Wipe | WITCH HAZEL | Diamond Wipes International, Inc | 4458c80c-d013-55ba-e063-6394a90a6b39 | 2025-11-24 | Warnings | 101I4J0U34 |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | beda35c3-9a8b-47ad-e053-2995a90a7b1b | 2025-11-24 | Warnings | 059QF0KO0R |
| Easy Care First Aid Eyewash | WATER | Tender Corporation | a070aac8-e6d2-ef10-e053-2a95a90aa5b1 | 2025-11-24 | Warnings | 059QF0KO0R |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | e07a064b-f680-405c-bbcd-24fac430951e | 2025-11-24 | Warnings | 059QF0KO0R |
| ULINE Eyewash | EYEWASH | Niagara Pharmaceuticals Inc. | 2d7f22d2-320b-6af1-e063-6294a90addc6 | 2025-11-24 | Warnings | 059QF0KO0R |
| Pur-Wash | EYEWASH | Niagara Pharmaceuticals, Inc. | 0d43b1c1-2699-37f1-e054-00144ff88e88 | 2025-11-24 | Warnings | 059QF0KO0R |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | 777e1559-786f-8d54-e053-2991aa0aa98d | 2025-11-24 | Warnings | 059QF0KO0R |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | 7289103a-5cbf-42f4-8848-e827149a43ca | 2025-11-24 | Warnings | 059QF0KO0R |
| Eyewash Additive Concentrate | WATER AND PROPYLENE GLYCOL | Haws Corporation | dd168403-398c-41ff-b1df-d93e4ff39de3 | 2025-11-20 | Warnings | 059QF0KO0R |
| Sterile Water | WATER | Fresenius Kabi USA, LLC | fd823bef-c14c-4708-a18a-8aaa8470412f | 2025-11-18 | Warnings, Adverse reactions | 059QF0KO0R |
| Eyesaline Eyewash Concentrate | PURIFIED WATER | Honeywell Safety Products USA, Inc. | 3765c251-eb14-d60f-e063-6294a90a6a4d | 2025-11-12 | Warnings | 059QF0KO0R |
| Eyesaline Emergency Eyewash | PURIFIED WATER | Honeywell Safety Products USA, Inc. | 37f244fd-c02f-e66a-e063-6394a90aed81 | 2025-11-12 | Warnings | 059QF0KO0R |
| Hazel Perineal Healing Foam | WITCH HAZEL | Jiangsu Senwo Medical Technology Co., Ltd. | 314b75cb-affe-a248-e063-6294a90a47b7 | 2025-11-07 | Warnings | 101I4J0U34 |
| STERILE WATER | WATER | Henry Schein, Inc. | f4087143-9868-4308-b96c-43657ee8ec28 | 2025-11-07 | Warnings, Adverse reactions | 059QF0KO0R |
| Bacteriostatic Water | BACTERIOSTATIC WATER | ProPharma Distribution | 42c6938e-f747-ae13-e063-6294a90a59a3 | 2025-11-04 | Warnings, Adverse reactions | 059QF0KO0R |
| Witch Hazel | WITCH HAZEL | Premier Brands of America Inc. | 38583c02-497b-922c-e063-6294a90a49de | 2025-11-03 | Warnings | 101I4J0U34 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.