Home NDC 84469-721 ESPOIR WATER SPLASH SUN SERUM
Product NDC 84469-721
11-digit product format 844690721
Labeler code 84469
Product ID 84469-721_3f724e4a-a6d4-f837-e063-6394a90ac084
Type HUMAN OTC DRUG
Nonproprietary name homosalate, octocrylene, octisalate, avobenzone
Dosage form LOTION
Route TOPICAL
Labeler ESPOIR Corporation
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-09-02
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength 30; 95; 45; 50 mg/mL; mg/mL; mg/mL; mg/mL
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 ESPOIR WATER SPLASH SUN SERUM
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 30 mg/mL HOMOSALATE 95 mg/mL OCTISALATE 45 mg/mL OCTOCRYLENE 50 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 84469-721-01 ESPOIR WATER SPLASH SUN SERUM 50 mL in 1 BOTTLE, PUMP LOTION 50 4 84469-721-01 ESPOIR WATER SPLASH SUN SERUM 1 in 1 BOX LOTION 1 4 84469-721-02 ESPOIR WATER SPLASH SUN SERUM 5 mL in 1 CONTAINER LOTION 5 4 84469-721-03 ESPOIR WATER SPLASH SUN SERUM 1 in 1 BOX LOTION 1 4 84469-721-03 ESPOIR WATER SPLASH SUN SERUM 2 in 1 BLISTER PACK LOTION 2 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 84469-721 ESPOIR WATER SPLASH SUN SERUM (HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE) LOTION [ESPOIR CORPORATION] 3 Current NDC, 5 package rows 20250323_1c4e7ba2-05e8-f949-e063-6394a90a699d.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 354 · 7,077 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 84469-721-01 84469072101 1 BOTTLE, PUMP in 1 BOX (84469-721-01) / 50 mL in 1 BOTTLE, PUMP 2024-09-02 No No Current 84469-721-02 84469072102 5 mL in 1 CONTAINER 5 ml Historical 84469-721-03 84469072103 2 BOX in 1 BLISTER PACK (84469-721-03) / 1 BOTTLE, PUMP in 1 BOX / 50 mL in 1 BOTTLE, PUMP 2 box 2025-12-01 No No Current