Home NDC 69842-083-01 Sport Sunstick SPF 30 Sunscreen
Product NDC 69842-083
Requested package NDC 69842-083-01
11-digit product format 698420083
Labeler code 69842
Product ID 69842-083_51e197be-8f55-40e7-ba69-f81ba388c08e
Type HUMAN OTC DRUG
Nonproprietary name avobenzone, octinoxate, octisalate
Dosage form STICK
Route TOPICAL
Labeler CVS Health
Application part352
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2017-04-01
Substance AVOBENZONE; OCTINOXATE; OCTISALATE
Active strength 20; 75; 30 mg/g; mg/g; mg/g
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 Sport Sunstick SPF 30 Sunscreen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 20 mg/g OCTINOXATE 75 mg/g OCTISALATE 30 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination G63QQF2NOX Internal UNII lookup 4Y5P7MUD51 Internal UNII lookup 4X49Y0596W 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 69842-083-01 Sport Sunstick SPF 30 Sunscreen 7 g in 1 CASE STICK 7 1 69842-083-01 Sport Sunstick SPF 30 Sunscreen 1 in 1 BLISTER PACK STICK 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69842-083 SPORT SUNSTICK SPF 30 SUNSCREEN (AVOBENZONE, OCTINOXATE, OCTISALATE) STICK [CVS HEALTH] 1 Current NDC, Legacy NDC, 2 package rows 20170420_2dda092d-cc09-468c-a805-7a7f78827d44.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 1 of 1 · 1 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 69842-083-01 69842008301 1 CASE in 1 BLISTER PACK (69842-083-01) / 7 g in 1 CASE 1 case 2017-04-01 0000-00-00 No No Current