NDC 69384-080-01 - HAIRJOY EYELASH SIGNATURE
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
- 69384-080
- Requested NDC
- 69384-080-01
- Package NDCs from labels
- 69384-080-01, 69384-080-02
- Manufacturer
- HAIRJOY | Ester Co., Ltd.
- Effective date
- 2020-10-23
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| HAIRJOY EYELASH SIGNATURE - HAIRJOY | Ester Co., Ltd. | HAIRJOY | Ester Co., Ltd. | 2020-10-23 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 69384-080-02 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-7e75-a426-e053-dadaa90af4c2 | ca42d0a4-b9f8-48b9-bd4c-8c669e31e772 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69384-080-01 | HAIRJOY EYELASH SIGNATURE | 15 mL in 1 CONTAINER | LIQUID | 15 | 1 | |
| 69384-080-02 | HAIRJOY EYELASH SIGNATURE | 1 in 1 CARTON | LIQUID | 1 | 1 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
| CVS Hand Sanitizer | ALCOHOL | CVS | d0081c50-c0d2-436a-ba83-5d1982ae64b7 | 2015-08-17 | Warnings | 3K9958V90M |
| Instant Hand Sanitizer | ALCOHOL | Safetec of America, Inc. | f9e30645-491b-4f54-acfd-f863ee235607 | 2013-08-07 | Warnings | 3K9958V90M |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.