NDC 69142-001-01 - Breast Essence II
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
- 69142-001
- Requested NDC
- 69142-001-01
- Package NDCs from labels
- 69142-001-01, 69142-001-02
- Manufacturer
- yeojaya
- Effective date
- 2014-07-29
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Breast Essence II - yeojaya | yeojaya | 2014-07-29 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 69142-001-02 | 2019-11-27 | C162847 | 48780-1 | 9855e2a2-3f54-60a7-e053-dbdaa90a05bd | Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69142-001-01 | Breast Essence II | 50 mL in 1 BOTTLE, WITH APPLICATOR | CREAM | 50 | 1 | |
| 69142-001-02 | Breast Essence II | 1 in 1 CARTON | CREAM | 1 | 1 |
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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| MAXIMUM STRENGTH ANTACID ANTIGAS | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE | WALGREEN COMPANY | 7cd8fdf4-f762-f936-e053-2a91aa0aa6ee | 2025-11-19 | Warnings | 92RU3N3Y1O |
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| Softlips Vanilla | DIMETHICONE, OCTINOXATE, OCTISALATE, OXYBENZONE | The Mentholatum Company | 8dff782f-7201-4ad9-94d2-672058f817b8 | 2025-11-19 | Warnings | 92RU3N3Y1O |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.