Tinted Liplux
- Product NDC
- 76150-315
- Requested package NDC
- 76150-315-32
- 11-digit product format
- 761500315
- Labeler code
- 76150
- Product ID
- 76150-315_c7a34f35-0c2a-6dbf-e053-2995a90a4775
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SPF 30 Classic
- Dosage form
- LIPSTICK
- Route
- TOPICAL
- Labeler
- Bell International Laboratories, Inc
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2021-07-21
- Marketing end
- 0000-00-00
- Substance
- OCTISALATE; OCTOCRYLENE; AVOBENZONE
- Active strength
- 5 g/100g; g/100g; g/100g
- 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 |
|---|---|---|---|---|---|---|---|---|
| 76150-315-32 | 76150031532 | 4.2 g in 1 TUBE (76150-315-32) | 4.2 g | 2021-07-21 | 0000-00-00 | No | No | Current |