SUGARGIRL SET SPF 30 SUNSCREEN SHIMMER SUNSCREEN MIST FOR THE FACE- homosalate, octocrylene, octisalate, avobenzone liquid

Sugargirl Set SPF 30 Sunscreen Shimmer Sunscreen Mist For the Face by

Drug Labeling and Warnings

Sugargirl Set SPF 30 Sunscreen Shimmer Sunscreen Mist For the Face by is a Otc medication manufactured, distributed, or labeled by I World LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

Homosalate 15%, Octocrylene 10%, Octisalate 5%, Avobenzone 3%

Purpose

Sunscreen

Uses

• Helps prevent sunburn.

Warnings

For external use only.
Skin cancer/skin aging alert

• Spending time in the sun increases your risk of skin cancer and early skin aging.
• This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.

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 product is swallowed get medical help or contact a poison control centre right away.

Directions

• Apply generously and evenly 15 minutes before sun exposer.
• Reapply at least every 2 hours.
• Use a water resistant sunscreen if swimming or sweating.
• Children under 6 month: ask a doctor.

Other information

Protect the product in this container from excessive heat and direct sun.

Inactive ingredients

ALCOHOL, BUTYLOCTYL SALICYLATE, WATER, DIISOPROPYL ADIPATE, LAURYL LACTATE, DICAPRYLYL CARBONATE, TRIETHYL CITRATE, FRAGRANCE, TOCOPHERYL ACETATE, ACRYLATES/OCTYLACRYLAMIDE COPOLYMER, SYNTHETIC FLUORPHLOGOPITE, MICA, TITANIUM DIOXIDE(CI 77891), IRON OXIDES (CI 77491).

Questions or comments?

1-212-244-5170  info@amora.beauty

Package Labeling:

INGREDIENTS AND APPEARANCE

SUGARGIRL SET SPF 30 SUNSCREEN SHIMMER SUNSCREEN MIST FOR THE FACE 
homosalate, octocrylene, octisalate, avobenzone liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85179-043
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	150 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	100 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (ETHYLHEXYL SALICYLATE - UNII:4X49Y0596W)	OCTISALATE	50 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
WATER (UNII: 059QF0KO0R)
DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
LAURYL LACTATE (UNII: G5SU0BFK7O)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (40000 MW) (UNII: 7LL6SY9YFV)
MICA (UNII: V8A1AW0880)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
FERRIC OXIDE RED (UNII: 1K09F3G675)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85179-043-00	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/06/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	12/06/2025

Labeler - I World LLC (830590126)

Registrant - I World LLC (830590126)