Bath and Body Works SPF

Product NDC
62670-6689
11-digit product format
626706689
Labeler code
62670
Product ID
62670-6689_4c0ce9fb-6a89-b622-e063-6394a90a7e87
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone,Homosalate,Octisalate,Octocrylene
Dosage form
SPRAY
Route
TOPICAL
Labeler
Bath & Body Works, Inc.
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-02-12
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
3; 10; 5; 10 mg/100mg; mg/100mg; mg/100mg; mg/100mg
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Bath and Body Works SPF
Brand name suffix
Waikiki Beach Coconut
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE3 mg/100mg
HOMOSALATE10 mg/100mg
OCTISALATE5 mg/100mg
OCTOCRYLENE10 mg/100mg

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG63QQF2NOX, V06SV4M95S, 4X49Y0596W, 5A68WGF6WM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62670-6689-0Bath and Body Works SPFWaikiki Beach Coconut117 mg in 1 CANSPRAY1173
62670-6689-1Bath and Body Works SPFWaikiki Beach Coconut53 mg in 1 CANSPRAY533

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62670-6689BATH AND BODY WORKS SPF WAIKIKI BEACH COCONUT (AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE) SPRAY [BATH & BODY WORKS, INC.]1Current NDC, 2 package rows20240703_1c37b8d7-de72-f534-e063-6294a90aeab7.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
62670-6689-062670668900117 mg in 1 CAN (62670-6689-0) 117 mg2024-02-12NoNoHistorical
62670-6689-16267066890153 mg in 1 CAN (62670-6689-1) 53 mg2025-02-10NoNoHistorical