NDC 73676-216-20 - Abib No White Cast SPF Gift Set
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
- 73676-216
- Requested NDC
- 73676-216-20
- Package NDCs from labels
- 73676-216-20, 73676-216-40
- Manufacturer
- FOURCOMPANY CO., LTD. | Cosmax, Inc.
- Effective date
- 2026-06-04
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Abib Airy clear sunscreen gel Smoothing tube | FOURCOMPANY CO., LTD. | Cosmax, Inc. | 2026-06-04 | HUMAN OTC DRUG LABEL |
| Abib Quick Sunstick Protection Bar | FOURCOMPANY CO., LTD. | Cosmax, Inc. | 2026-03-30 | HUMAN OTC DRUG LABEL |
| Abib Quick & Airy sunstick Duo set | FOURCOMPANY CO., LTD. | Cosmax, Inc. | 2025-05-02 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73676-216-20 | Abib Quick sunstick Protection bar | 22 g in 1 CONTAINER | STICK | 22 | 4 | |
| 73676-216-40 | Abib Quick sunstick Protection bar | 1 in 1 BOX | STICK | 1 | 4 | |
| 73676-216-20 | ABIB QUICK AND AIRY SUNSTICK DUO SET | 22 g in 1 CONTAINER | STICK | 22 g in 55 | 4.5 g in 100g | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 73676-216 | ABIB QUICK SUNSTICK PROTECTION BAR (HOMOSALATE,OCTOCRYLENE,OCTISALATE,AVOBENZONE) STICK [FOURCOMPANY CO., LTD.] | 2 | Current NDC, 2 package rows | 20250413_1a2ab632-643f-1aa9-e063-6394a90a0c05.zip |
| 73676-216 | ABIB QUICK AND AIRY SUNSTICK DUO SET (HOMOSALATE, OCTOCRYLENE,OCTISALATE,AVOBENZONE) KIT [FOURCOMPANY CO., LTD.] | 1 | Current NDC | 20250524_34292261-4d05-e07d-e063-6294a90a4741.zip |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.