Home NDC 81159-131 SEAWEED BATH CO. SPF 50 SPORT
Product NDC 81159-131
11-digit product format 811590131
Labeler code 81159
Product ID 81159-131_09e25fad-8fe9-b0f7-e063-6294a90a20e8
Type HUMAN OTC DRUG
Nonproprietary name OCTOCRYLENE, ZINC OXIDE, OCTISALATE
Dosage form LOTION
Route TOPICAL
Labeler The Seaweed Bath Co.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-11-23
Substance OCTOCRYLENE; ZINC OXIDE; OCTISALATE
Active strength 100; 85; 50 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 SEAWEED BATH CO. SPF 50 SPORT
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTOCRYLENE 100 mg/mL ZINC OXIDE 85 mg/mL OCTISALATE 50 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5A68WGF6WM Internal UNII lookup SOI2LOH54Z 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 81159-131-00 SEAWEED BATH CO. SPF 50 SPORT 100 mL in 1 TUBE LOTION 100 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81159-131 SEAWEED BATH CO. SPF 50 SPORT (OCTOCRYLENE, ZINC OXIDE, OCTISALATE) LOTION [THE SEAWEED BATH CO.] 2 Current NDC, Legacy NDC, 1 package rows 20231112_f01516bf-8aed-4402-a3f9-ef11c54d46b3.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 27 of 353 · 7,049 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 81159-131-00 81159013100 100 mL in 1 TUBE (81159-131-00) 100 ml 2020-11-23 0000-00-00 No No Current