Hampton Sun SPF 50

Product NDC
87170-020
11-digit product format
871700020
Labeler code
87170
Product ID
87170-020_5219c8eb-a16a-5834-e063-6394a90a0a71
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone 3.00 % Octisalate 5.00 % Homosalate 10.00 %
Dosage form
SPRAY
Route
TOPICAL
Labeler
S&C Hampton Sun LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-06-25
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
Hampton Sun 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
87170-020-05Hampton Sun SPF 50142 g in 1 CANSPRAY1422

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
87170-020-0587170002005142 g in 1 CAN (87170-020-05) 142 g2022-06-25NoNoCurrent