Home NDC 62670-7002 Bath and Body Works SPF
Product NDC 62670-7002
11-digit product format 626707002
Labeler code 62670
Product ID 62670-7002_5606b9c0-cf37-38ca-e063-6294a90a550a
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone,Homosalate,Octisalate
Dosage form STICK
Route TOPICAL
Labeler Bath & Body Works, Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-05-04
Substance AVOBENZONE; HOMOSALATE; OCTISALATE
Active strength 2.5; 10; 5 mg/100mg; mg/100mg; mg/100mg
NDC exclude flag No
Listing certified through 2027-12-31
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 Bronze Kiss
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 2.5 mg/100mg HOMOSALATE 10 mg/100mg OCTISALATE 5 mg/100mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination G63QQF2NOX Internal UNII lookup V06SV4M95S Internal UNII lookup 4X49Y0596W Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 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 62670-7002-0 62670700200 4000 mg in 1 APPLICATOR (62670-7002-0) 4000 mg 2026-05-04 No No Current