Jack Black
- Product NDC
- 66738-941
- 11-digit product format
- 667380941
- Labeler code
- 66738
- Product ID
- 66738-941_5b771335-1d5a-12be-e063-6394a90a1f2c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone/Homosalate/Octisalate/Petrolatum
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Jack Black L.L.C.
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-01
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; PETROLATUM
- Active strength
- 3; 10; 5; 40.2 g/100mL; g/100mL; g/100mL; g/100mL
- 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
- Jack Black
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| AVOBENZONE | 3 g/100mL |
| HOMOSALATE | 10 g/100mL |
| OCTISALATE | 5 g/100mL |
| PETROLATUM | 40.2 g/100mL |
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 |
|---|---|---|---|---|---|---|---|
| 66738-941-01 | 66738094101 | 1 TUBE in 1 CARTON (66738-941-01) / 7 mL in 1 TUBE (66738-941-21) | 1 tube | 2026-09-01 | No | No | Current |