Home NDC 71239-845 Ola Botanicals Sunscreen SPF 30
Product NDC 71239-845
11-digit product format 712390845
Labeler code 71239
Product ID 71239-845_3694282d-fa57-a94f-e063-6294a90a9ea8
Type HUMAN OTC DRUG
Nonproprietary name ZINC OXIDE
Dosage form LOTION
Route TOPICAL
Labeler Natural Health Partners, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-05-19
Substance ZINC OXIDE
Active strength 210 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 Ola Botanicals Sunscreen SPF 30
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 210 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup
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 71239-845-00 Ola Botanicals Sunscreen SPF 30 236 mL in 1 BOTTLE LOTION 236 1
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 81 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 71239-845-00 71239084500 236 mL in 1 BOTTLE (71239-845-00) 236 ml 2025-05-19 No No Current