Home NDC 66738-221 Jack Black L.L.C.
Product NDC 66738-221
11-digit product format 667380221
Labeler code 66738
Product ID 66738-221_3e0eb291-6bdb-2f26-e063-6294a90ac466
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 2025-10-01
Substance AVOBENZONE; PETROLATUM; OCTISALATE; HOMOSALATE
Active strength 3; 40.2; 5; 10 g/100mL; g/100mL; g/100mL; g/100mL
NDC exclude flag No
Listing certified through 2026-12-31
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 L.L.C.
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 3 g/100mL PETROLATUM 40.2 g/100mL OCTISALATE 5 g/100mL HOMOSALATE 10 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 66738-221-01 Jack Black L.L.C. 1 in 1 CARTON OINTMENT 1 1 66738-221-21 Jack Black L.L.C. 7 mL in 1 TUBE OINTMENT 7 1
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.
Matched openFDA labels page 81 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 66738-221-01 66738022101 1 TUBE in 1 CARTON (66738-221-01) / 7 mL in 1 TUBE (66738-221-21) 1 tube 2025-10-01 No No Current 66738-221-21 66738022121 7 mL in 1 TUBE 7 ml Historical