Home NDC 66738-020 Double-Duty Face Moisturizer
Product NDC 66738-020
11-digit product format 667380020
Labeler code 66738
Product ID 66738-020_5aff192a-cd63-e163-e063-6294a90ab621
Type HUMAN OTC DRUG
Nonproprietary name mositurizing sunscreen
Dosage form LOTION
Route TOPICAL
Labeler Jack Black, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2009-05-29
Substance AVOBENZONE; OCTINOXATE
Active strength 2.2; 7.5 g/1000g; g/1000g
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 Double-Duty Face Moisturizer
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 2.2 g/1000g OCTINOXATE 7.5 g/1000g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination G63QQF2NOX Internal UNII lookup 4Y5P7MUD51 Internal UNII lookup
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 66738-020-01 Double-Duty Face Moisturizer 30 g in 1 TUBE LOTION 30 8 66738-020-02 Double-Duty Face Moisturizer 2 g in 1 PACKET LOTION 2 8 66738-020-03 Double-Duty Face Moisturizer 97 g in 1 BOTTLE LOTION 97 8 66738-020-04 Double-Duty Face Moisturizer 44 g in 1 TUBE LOTION 44 8 66738-020-16 Double-Duty Face Moisturizer 480 g in 1 BOTTLE LOTION 480 8 66738-020-19 Double-Duty Face Moisturizer 251 g in 1 BOTTLE LOTION 251 8 66738-020-50 Double-Duty Face Moisturizer 14 g in 1 TUBE LOTION 14 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 66738-020 DOUBLE-DUTY FACE MOISTURIZER (MOSITURIZING SUNSCREEN) LOTION [JACK BLACK, LLC] 8 Current NDC, Legacy NDC, 7 package rows 20231109_672be406-e3a1-47b4-8ef6-ee2b62baae96.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 26 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 66738-020-01 66738002001 30 g in 1 TUBE (66738-020-01) 30 g 2020-04-01 0000-00-00 No No Current 66738-020-02 66738002002 2 g in 1 PACKET (66738-020-02) 2 g 2020-03-11 0000-00-00 No No Current 66738-020-03 66738002003 97 g in 1 BOTTLE (66738-020-03) 97 g 2009-05-29 0000-00-00 No No Current 66738-020-04 66738002004 44 g in 1 TUBE (66738-020-04) 44 g 2009-07-30 0000-00-00 No No Current 66738-020-16 66738002016 480 g in 1 BOTTLE (66738-020-16) 480 g 2020-05-01 0000-00-00 No No Current 66738-020-19 66738002019 251 g in 1 BOTTLE (66738-020-19) 251 g 2011-06-15 0000-00-00 No No Current 66738-020-50 66738002050 14 g in 1 TUBE (66738-020-50) 14 g 2020-03-11 0000-00-00 No No Current