Kids Sunscreen SPF 50

Product NDC
49757-011
11-digit product format
497570011
Labeler code
49757
Product ID
49757-011_4d517e32-9b88-dcf3-e063-6394a90ab83d
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone 3% , Homosalate 10%,Octisalate 5%
Dosage form
SPRAY
Route
TOPICAL
Labeler
Rocky Mountain
Application
M20
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-08-21
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE
Active strength
3; 10; 5 g/100g; g/100g; g/100g
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Kids Sunscreen SPF 50
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE3 g/100g
HOMOSALATE10 g/100g
OCTISALATE5 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG63QQF2NOX, V06SV4M95S, 4X49Y0596W

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49757-011-09Kids Sunscreen SPF 50453 g in 1 CONTAINERSPRAY4533
49757-011-12Kids Sunscreen SPF 50907 g in 1 CONTAINERSPRAY9073
49757-011-22Kids Sunscreen SPF 503629 g in 1 CONTAINERSPRAY36293

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
49757-011-0949757001109453 g in 1 CONTAINER453 gHistorical
49757-011-1249757001112907 g in 1 CONTAINER (49757-011-12) 907 g2025-08-21NoNoCurrent
49757-011-22497570011223629 g in 1 CONTAINER (49757-011-22) 3629 g2025-08-21NoNoCurrent