Home NDC 80641-021 Vacation Classic Whip SPF 50
Product NDC 80641-021
11-digit product format 806410021
Labeler code 80641
Product ID 80641-021_36d75da5-db6c-63f7-e063-6394a90ac193
Type HUMAN OTC DRUG
Nonproprietary name Homosalate, Octisalate, Octocrylene, Avobenzone
Dosage form AEROSOL, FOAM
Route TOPICAL
Labeler Vacation Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-06-04
Substance OCTISALATE; HOMOSALATE; OCTOCRYLENE; AVOBENZONE
Active strength .05; .15; .05; .03 g/g; g/g; g/g; g/g
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 Vacation Classic Whip SPF 50
Brand name suffix Broad Spectrum SPF 50
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE .05 g/g HOMOSALATE .15 g/g OCTOCRYLENE .05 g/g AVOBENZONE .03 g/g
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 Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 80641-021-02 Vacation Classic Whip SPF 50Broad Spectrum SPF 50 113 g in 1 CAN AEROSOL, FOAM 113 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 45 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 80641-021-02 80641002102 113 g in 1 CAN (80641-021-02) 113 g 2025-06-04 No No Current