Belo Intensive Brightening
- Product NDC
- 82701-003
- 11-digit product format
- 827010003
- Labeler code
- 82701
- Product ID
- 82701-003_eea0e7c8-73eb-6d70-e053-2a95a90a7674
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octyl methoxycinnamate, Titanium dioxide, Octocrylene, Octinoxate
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Intelligent Skin Care Inc.
- Application
- M020
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2022-06-20
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; OCTOCRYLENE; OXYBENZONE; TITANIUM DIOXIDE
- Active strength
- 12 mg/200mg; mg/200mg; mg/200mg; mg/200mg
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
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.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 82701-003-01 | 82701000301 | 200 mg in 1 TUBE (82701-003-01) | 200 mg | 2022-06-20 | 0000-00-00 | No | No | Current |