Home NDC 61973-106 Arizona Sun Sunscreen Kids Water Resistant SPF 30
Product NDC 61973-106
11-digit product format 619730106
Labeler code 61973
Product ID 61973-106_4f0c6096-de37-13b1-e063-6394a90a7ec1
Type HUMAN OTC DRUG
Nonproprietary name Sunscreen
Dosage form LOTION
Route TOPICAL
Labeler Arizona Sun Products
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-02-15
Substance OXYBENZONE; OCTINOXATE; AVOBENZONE; OCTISALATE; HOMOSALATE
Active strength 30; 75; 30; 50; 50 mg/g; mg/g; mg/g; mg/g; mg/g
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 Arizona Sun Sunscreen Kids Water Resistant SPF 30
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OXYBENZONE 30 mg/g OCTINOXATE 75 mg/g AVOBENZONE 30 mg/g OCTISALATE 50 mg/g HOMOSALATE 50 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 5 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 61973-106-01 Arizona Sun Sunscreen Kids Water Resistant SPF 30 30 g in 1 BOTTLE LOTION 30 2 61973-106-04 Arizona Sun Sunscreen Kids Water Resistant SPF 30 120 g in 1 BOTTLE LOTION 120 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 61973-106 ARIZONA SUN SUNSCREEN KIDS WATER RESISTANT SPF 30 (SUNSCREEN) LOTION [ARIZONA SUN PRODUCTS] 1 Current NDC, 1 package rows 20240217_116ed17c-3b38-5e96-e063-6294a90a4246.zip 61973-106 ARIZONA SUN SUNSCREEN KIDS WATER RESISTANT SPF 30 (SUNSCREEN) LOTION [ARIZONA SUN PRODUCTS] 1 Current NDC, 1 package rows 20240217_116e71c4-f443-0b6c-e063-6394a90a0cdd.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 Sample Exclude flag Status 61973-106-01 61973010601 30 g in 1 BOTTLE (61973-106-01) 30 g 2024-02-15 No No Current 61973-106-04 61973010604 120 g in 1 BOTTLE (61973-106-04) 120 g 2024-02-15 No No Current