Home NDC 66738-304 Jack Black Sun Guard Sunscreen SPF45
Product NDC 66738-304
11-digit product format 667380304
Labeler code 66738
Product ID 66738-304_5aff7e41-58cf-5ab8-e063-6294a90aa1c7
Type HUMAN OTC DRUG
Nonproprietary name Sunscreen
Dosage form LOTION
Route TOPICAL
Labeler Jack Black, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2010-02-09
Substance OCTISALATE; OCTINOXATE; ZINC OXIDE
Active strength 3; 7.5; 8 g/1000g; g/1000g; g/1000g
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
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 Sun Guard Sunscreen SPF45
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 3 g/1000g OCTINOXATE 7.5 g/1000g ZINC OXIDE 8 g/1000g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4X49Y0596W Internal UNII lookup 4Y5P7MUD51 Internal UNII lookup SOI2LOH54Z Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 66738-304-14 Jack Black Sun Guard Sunscreen SPF45 113 g in 1 TUBE LOTION 113 4 66738-304-27 Jack Black Sun Guard Sunscreen SPF45 44 g in 1 TUBE LOTION 44 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 66738-304 JACK BLACK SUN GUARD SUNSCREEN SPF45 (SUNSCREEN) LOTION [JACK BLACK, LLC] 4 Current NDC, Legacy NDC, 2 package rows 20231109_3cc86bb2-05ce-47eb-8c71-f4f116ca5840.zip
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 Marketing end Sample Exclude flag Status 66738-304-14 66738030414 113 g in 1 TUBE (66738-304-14) 113 g 2010-02-09 0000-00-00 No No Current 66738-304-27 66738030427 44 g in 1 TUBE (66738-304-27) 44 g 2013-02-04 0000-00-00 No No Current