Every Sun Day Ultra-Sheer Priming Sunscreen Stick

Product NDC
49404-155
11-digit product format
494040155
Labeler code
49404
Product ID
49404-155_2cc68544-e513-f895-e063-6394a90aa577
Type
HUMAN OTC DRUG
Nonproprietary name
avobenzone,homosalate,octisalate,octocrylene
Dosage form
STICK
Route
TOPICAL
Labeler
Have & Be Co., Ltd.
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-01-10
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
30; 65; 45; 65 mg/g; mg/g; mg/g; mg/g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Every Sun Day Ultra-Sheer Priming Sunscreen Stick
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE30 mg/g
HOMOSALATE65 mg/g
OCTISALATE45 mg/g
OCTOCRYLENE65 mg/g

Harmonized Identifiers#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49404-155-01Every Sun Day Ultra-Sheer Priming Sunscreen Stick1 in 1 CARTONSTICK12
49404-155-01Every Sun Day Ultra-Sheer Priming Sunscreen Stick19 g in 1 CONTAINERSTICK192

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49404-155EVERY SUN DAY ULTRA-SHEER PRIMING SUNSCREEN STICK (AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE) STICK [HAVE & BE CO., LTD.]2Current NDC, 2 package rows20250130_2b53aa68-9c05-1682-e063-6294a90a968c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
49404-155-01494040155011 CONTAINER in 1 CARTON (49404-155-01) / 19 g in 1 CONTAINER1 container2025-01-10NoNoCurrent