NDC 68828-705-01 - Jafra Daily Sensitive Skin Antiperspirant Deodorant Roll-on
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
- 68828-705
- Requested NDC
- 68828-705-01
- Package NDCs from labels
- 68828-705-01, 68828-705-02
- Manufacturer
- Distribuidora Comercial Jafra, S.A. de C.V. | Jafra Cosmetics International Inc.
- Effective date
- 2025-01-02
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Jafra Daily Sensitive Skin Antiperspirant Deodorant Roll-on | Distribuidora Comercial Jafra, S.A. de C.V. | Jafra Cosmetics International Inc. | 2025-01-02 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68828-705-01 | Jafra Daily Sensitive Skin Antiperspirant Deodorant Roll-on | 60 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 60 | 5 | |
| 68828-705-02 | Jafra Daily Sensitive Skin Antiperspirant Deodorant Roll-on | 1 in 1 CARTON | LIQUID | 1 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 68828-705 | JAFRA DAILY SENSITIVE SKIN ANTIPERSPIRANT DEODORANT ROLL-ON (ALUMINUM CHLOROHYDRATE) LIQUID [DISTRIBUIDORA COMERCIAL JAFRA, S.A. DE C.V.] | 5 | Current NDC, Legacy NDC, 2 package rows | 20250104_0d9b13ff-cd3f-477b-bda4-40e1076584b3.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.