Sun Bum Daily Body

Product NDC
69039-663
11-digit product format
690390663
Labeler code
69039
Product ID
69039-663_3f7f1343-719a-8676-e063-6394a90a4cda
Type
HUMAN OTC DRUG
Nonproprietary name
AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Dosage form
LOTION
Route
TOPICAL
Labeler
Sun Bum, LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-02-26
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
30; 80; 50; 90 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Sun Bum Daily Body
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE30 mg/mL
HOMOSALATE80 mg/mL
OCTISALATE50 mg/mL
OCTOCRYLENE90 mg/mL

Harmonized Identifiers#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69039-663-01Sun Bum Daily Body237 mL in 1 BOTTLE, PLASTICLOTION2375

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
69039-663-0169039066301237 mL in 1 BOTTLE, PLASTIC (69039-663-01) 237 ml2024-02-26NoNoCurrent