Burn Cream
- Product NDC
- 58228-7080
- 11-digit product format
- 582287080
- Labeler code
- 58228
- Product ID
- 58228-7080_5dc00980-1217-3bbd-e063-6294a90a0a02
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride, Lidocaine HCI
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Prostat First Aid
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-01-13
- Substance
- BENZALKONIUM CHLORIDE; LIDOCAINE HYDROCHLORIDE
- Active strength
- .0013; .005 g/g; g/g
- Pharmacologic classes
- Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Burn Cream
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| BENZALKONIUM CHLORIDE | .0013 g/g |
| LIDOCAINE HYDROCHLORIDE | .005 g/g |
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 | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 58228-7080-1 | 58228708001 | 25 PACKET in 1 BOX (58228-7080-1) / .9 g in 1 PACKET | 25 packet | 2026-01-13 | No | No | Current |