NDC 70157-021-01 - Bondi Sands Broad Spectrum SPF 60 Sunny Cream Body
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
- 70157-021
- Requested NDC
- 70157-021-01
- Package NDCs from labels
- 70157-021-01, 70157-021-02, 70157-021-03
- Manufacturer
- Baxter Laboratories Pty. Ltd.
- Effective date
- 2026-10-20
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Bondi Sands Broad Spectrum SPF 60 Sunny Cream Body Lotion | Baxter Laboratories Pty. Ltd. | 2026-10-20 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70157-021-01 | Bondi Sands Broad Spectrum SPF 60 Sunny Cream Body | 150 mL in 1 TUBE | LOTION | 150 | 2 | |
| 70157-021-02 | Bondi Sands Broad Spectrum SPF 60 Sunny Cream Body | 1 in 1 CARTON | LOTION | 1 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70157-021 | BONDI SANDS BROAD SPECTRUM SPF 60 SUNNY CREAM BODY (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [BAXTER LABORATORIES PTY. LTD.] | 1 | Current NDC, 2 package rows | 20241212_2861453a-12e9-faeb-e063-6394a90a527c.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.