Home NDC 62670-6868 Bath and Body Works SPF
Product NDC 62670-6868
11-digit product format 626706868
Labeler code 62670
Product ID 62670-6868_38d04b01-4363-ce12-e063-6294a90ad95d
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone,Homosalate,Octisalate,Octocrylene
Dosage form LOTION
Route TOPICAL
Labeler Bath & Body Works, Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-02-10
Substance OCTOCRYLENE; AVOBENZONE; HOMOSALATE; OCTISALATE
Active strength 10; 3; 10; 5 mg/100mg; mg/100mg; mg/100mg; mg/100mg
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 Bath and Body Works SPF
Brand name suffix Tahiti Isle
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTOCRYLENE 10 mg/100mg AVOBENZONE 3 mg/100mg HOMOSALATE 10 mg/100mg OCTISALATE 5 mg/100mg
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 62670-6868-0 Bath and Body Works SPFTahiti Isle 74 mg in 1 BOTTLE LOTION 74 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 27 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 62670-6868-0 62670686800 74 mg in 1 BOTTLE (62670-6868-0) 74 mg 2025-02-10 No No Current