Apeaz Ultra
- Product NDC
- 15478-111
- 11-digit product format
- 154780111
- Labeler code
- 15478
- Product ID
- 15478-111_3560957d-2a24-4eec-9e19-a572d501d5ed
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- camphor (synthetic), menthol, and methyl salicylate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Topical Pharmaceuticals Inc.
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-02-05
- Marketing end
- 0000-00-00
- Substance
- CAMPHOR (SYNTHETIC); MENTHOL; METHYL SALICYLATE
- Active strength
- 40 mg/g; mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|---|---|---|---|---|---|---|---|
| 15478-111-04 | 15478011104 | 1 CONTAINER in 1 CARTON (15478-111-04) > 56.7 g in 1 CONTAINER | 1 container | 2018-02-05 | 0000-00-00 | No | No | Current |