NDC 52891-103-01 - DR. OBERON NATURAL BABY
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
- 52891-103
- Requested NDC
- 52891-103-01
- Package NDCs from labels
- 52891-103-01, 52891-103-02
- Manufacturer
- Oberon Cosmetic Co., Ltd.
- Effective date
- 2014-06-29
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| DR. OBERON NATURAL BABY LOTION | Oberon Cosmetic Co., Ltd. | 2014-06-29 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 52891-103-02 | 2019-11-27 | C162847 | 48780-1 | 9855e2a2-4dcd-60a7-e053-dbdaa90a05bd | DR. OBERON NATURAL BABY LOTION |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 52891-103-01 | DR. OBERON NATURAL BABY | 50 mL in 1 TUBE | LOTION | 50 | 2 | |
| 52891-103-02 | DR. OBERON NATURAL BABY | 1 in 1 CARTON | LOTION | 1 | 2 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
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.