Habit
- Product NDC
- 76150-261
- 11-digit product format
- 761500261
- Labeler code
- 76150
- Product ID
- 76150-261_b7c7cb59-607e-3fd7-e053-2a95a90af558
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Facial
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Bell International Laboratories, Inc
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-01-01
- Marketing end
- 0000-00-00
- Substance
- OCTISALATE; AVOBENZONE; HOMOSALATE; OCTOCRYLENE
- Active strength
- 5 g/100mL; g/100mL; g/100mL; g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 76150-261-51 | 76150026151 | 30 mL in 1 BOTTLE, PLASTIC (76150-261-51) | 30 ml | 2020-01-01 | 0000-00-00 | No | No | Current |