Home NDC 81746-183 ZITSTICKA MEGASHADE SUNSCREEN SERUM (SPF-50)
Product NDC 81746-183
11-digit product format 817460183
Labeler code 81746
Product ID 81746-183_09e29758-29ad-1153-e063-6394a90ab827
Type HUMAN OTC DRUG
Nonproprietary name HOMOSALATE, OCTINOXATE, OCTISALATE, ZINC OXIDE
Dosage form LIQUID
Route TOPICAL
Labeler ZITSTICKA, Inc
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-04-10
Substance HOMOSALATE; OCTINOXATE; OCTISALATE; ZINC OXIDE
Active strength 75; 75; 50; 30 mg/mL; mg/mL; mg/mL; mg/mL
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
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 ZITSTICKA MEGASHADE SUNSCREEN SERUM (SPF-50)
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 75 mg/mL OCTINOXATE 75 mg/mL OCTISALATE 50 mg/mL ZINC OXIDE 30 mg/mL
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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 81746-183-00 ZITSTICKA MEGASHADE SUNSCREEN SERUM (SPF-50) 1 in 1 BOX LIQUID 1 3 81746-183-00 ZITSTICKA MEGASHADE SUNSCREEN SERUM (SPF-50) 50 mL in 1 BOTTLE, DROPPER LIQUID 50 3 81746-183-01 ZITSTICKA MEGASHADE SUNSCREEN SERUM (SPF-50) 1 in 1 BOX LIQUID 1 3 81746-183-01 ZITSTICKA MEGASHADE SUNSCREEN SERUM (SPF-50) 30 mL in 1 BOTTLE, DROPPER LIQUID 30 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81746-183 ZITSTICKA MEGASHADE SUNSCREEN SERUM (SPF-50) (HOMOSALATE, OCTINOXATE, OCTISALATE, ZINC OXIDE) LIQUID [ZITSTICKA, INC] 3 Current NDC, Legacy NDC, 4 package rows 20231112_32164318-7a7e-40b2-99da-8246c99fdbd3.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 Marketing start Marketing end Sample Exclude flag Status 81746-183-00 81746018300 1 BOTTLE, DROPPER in 1 BOX (81746-183-00) / 50 mL in 1 BOTTLE, DROPPER 2021-04-10 0000-00-00 No No Current 81746-183-01 81746018301 1 BOTTLE, DROPPER in 1 BOX (81746-183-01) / 30 mL in 1 BOTTLE, DROPPER 2021-09-01 0000-00-00 No No Current