FDA.reportPublic FDA data

Bath and Body Works SPF

Product NDC
62670-6688
11-digit product format
626706688
Labeler code
62670
Product ID
62670-6688_4f1fb381-9c1e-bcdc-e063-6394a90aad1e
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
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
62670-6688-0Bath and Body Works SPFWaikiki Beach Coconut117 mg in 1 BOTTLELOTION1173
62670-6688-1Bath and Body Works SPFWaikiki Beach Coconut74 mg in 1 BOTTLELOTION743

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62670-6688BATH AND BODY WORKS SPF WAIKIKI BEACH COCONUT (AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE) LOTION [BATH & BODY WORKS, INC.]1Current NDC, 2 package rows20240702_1c30de8a-4d29-bbac-e063-6294a90a84d9.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
62670-6688-062670668800117 mg in 1 BOTTLE (62670-6688-0) 117 mg2024-02-12NoNoHistorical
62670-6688-16267066880174 mg in 1 BOTTLE (62670-6688-1) 74 mg2024-02-12NoNoHistorical