NDC 83154-003-01 - ELROEL Pang Pang Sun Cushion S7
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
- 83154-003
- Requested NDC
- 83154-003-01
- Package NDCs from labels
- 83154-003-01, 83154-003-02, 83154-003-03, 83154-003-04, 83154-003-05, 83154-003-06, 83154-003-07, 83154-003-08, 83154-003-09, 83154-003-10
- Manufacturer
- MONOGLOT HOLDINGS Inc. | Cit Co., Ltd.
- Effective date
- 2026-04-17
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| 83154-003_ELROEL Pang Pang Sun Cushion S7 | MONOGLOT HOLDINGS Inc. | Cit Co., Ltd. | 2026-04-17 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 83154-003-01 | ELROEL Pang Pang Sun Cushion S7 | 25 g in 1 CONTAINER | CREAM | 25 | 10 | |
| 83154-003-02 | ELROEL Pang Pang Sun Cushion S7 | 1 in 1 CARTON | CREAM | 1 | 10 | |
| 83154-003-03 | ELROEL Pang Pang Sun Cushion S7 | 8 g in 1 CONTAINER | CREAM | 8 | 10 | |
| 83154-003-04 | ELROEL Pang Pang Sun Cushion S7 | 1 in 1 CARTON | CREAM | 1 | 10 | |
| 83154-003-05 | ELROEL Pang Pang Sun Cushion S7 | 15 g in 1 CONTAINER | CREAM | 15 | 10 | |
| 83154-003-06 | ELROEL Pang Pang Sun Cushion S7 | 1 in 1 CARTON | CREAM | 1 | 10 | |
| 83154-003-07 | ELROEL Pang Pang Sun Cushion S7 | 25 g in 1 CONTAINER | CREAM | 25 | 10 | |
| 83154-003-08 | ELROEL Pang Pang Sun Cushion S7 | 1 in 1 POUCH | CREAM | 1 | 10 | |
| 83154-003-09 | ELROEL Pang Pang Sun Cushion S7 | 15 g in 1 CONTAINER | CREAM | 15 | 10 | |
| 83154-003-10 | ELROEL Pang Pang Sun Cushion S7 | 1 in 1 POUCH | CREAM | 1 | 10 |
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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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.