Home NDC 73676-217 Abib Heartleaf mild sunscreen Relief tube
Product NDC 73676-217
11-digit product format 736760217
Labeler code 73676
Product ID 73676-217_34965587-c9b8-4066-e063-6394a90ab424
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form CREAM
Route TOPICAL
Labeler FOURCOMPANY CO., LTD.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-05-01
Substance ZINC OXIDE
Active strength 19.32 g/100mL
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 Abib Heartleaf mild sunscreen Relief tube
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 19.32 g/100mL
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 73676-217-01 Abib Heartleaf mild sunscreen Relief tube 50 mL in 1 TUBE CREAM 50 1 73676-217-02 Abib Heartleaf mild sunscreen Relief tube 1 in 1 CARTON CREAM 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73676-217 ABIB HEARTLEAF MILD SUNSCREEN RELIEF TUBE (ZINC OXIDE) CREAM [FOURCOMPANY CO., LTD.] 1 Current NDC, 2 package rows 20250509_34965587-c9b7-4066-e063-6394a90ab424.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 128 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 73676-217-01 73676021701 50 mL in 1 TUBE 50 ml Historical 73676-217-02 73676021702 1 TUBE in 1 CARTON (73676-217-02) / 50 mL in 1 TUBE (73676-217-01) 1 tube 2025-05-01 No No Current