GOOD TIMES SPF 50 SUNSCREEN- homosalate, octocrylene, octisalate, avobenzone spray 
EVERYDAY GROUP LIMITED

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Good Times SPF 50 Sunscreen Spray

Drug Facts

Active ingredients

Homosalate 10% Octocrylene 5% Octisalate 5% Avobenzone 3%


Purpose

Sunscreen

Uses

Warnings

For external use only

May burst if heated. Do not pierce or incinerate, even after use. Pressurized container:

Do not use near heal, open flames or while smoking. Do not spray on an open flame or other ignition source.  Extermely Flammable:

Do not use

on damaged or broken skin

When using this product

keep out of eyes, rinse with water to remove

Stop use and ask a doctor

if rash occurs

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away

Directions

Shake well. Hold container 4 to 6 inches from skin to apply. • Apply liberally 15 minutes before sun exposure • • Spray on hands then apply to face. • Do not apply in windy conditions. • Use in well-ventilated area. • Reapply: • After 80 minutes of swimming or sweating • Immediately after towel drying • At least every 2 hours • Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: Limit time in the sun, especially from 10 a.m. to 2 p.m. • Wear long-sleeved shirts, pants, hats, and sunglasses • Children under 6 months of age: Ask a doctor Do not spray directly into face.Sun Protection Measures:

Inactive ingredients

SD Alcohol 40-B, Tocopheryl Acetate, VA/Butyl Maleate/Isobornyl Acrylate Copolymer, Carica Papaya (Papaya) Seed Oil, Fragrance, Helianthus Annuus (Sunflower) Seed Oil, Lonicera Japonica (Honeysuckle) Flower Extract

Other information

Protect from sunlight. Store below 86°F/30°C. Do not store at temperatures above 120°F/50C.

Package Labeling:

Label2

GOOD TIMES SPF 50 SUNSCREEN 
homosalate, octocrylene, octisalate, avobenzone spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72098-009
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE100 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE50 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
DIBUTYL MALEATE (UNII: 4X371TMK9K)  
PAPAYA SEED OIL (UNII: N4P40Z2DDB)  
SUNFLOWER OIL (UNII: 3W1JG795YI)  
LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72098-009-01150 mL in 1 CAN; Type 0: Not a Combination Product06/01/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02006/01/2023
Labeler - EVERYDAY GROUP LIMITED (664624682)

Revised: 12/2023
Document Id: 0c86bd59-1f25-763f-e063-6394a90af4f1
Set id: f40c6c4a-47a2-5dfe-e053-2995a90a3df3
Version: 2
Effective Time: 20231215
 
EVERYDAY GROUP LIMITED