Suntone
- Product NDC
- 13630-0219
- Requested package NDC
- 13630-0219-4
- 11-digit product format
- 136300219
- Labeler code
- 13630
- Product ID
- 13630-0219_d60874f7-4dfc-4ba0-e053-2995a90a8d1a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Homosalate, Octisalate, Octocrylene
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Prime Packaging, Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-12-14
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 25 mg/mL; mg/mL; mg/mL; mg/mL
- 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.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 13630-0219-4 | 13630021904 | 185 mL in 1 CAN (13630-0219-4) | 185 ml | 2017-12-14 | 0000-00-00 | No | No | Current |