SUGARGIRL GLOW UP BODY ILLUMINATOR SHIMMER SUNSCREEN SPF 30- homosalate, octocrylene, octisalate, avobenzone gel

Sugargirl Glow Up Body Illuminator Shimmer Sunscreen SPF 30 by

Drug Labeling and Warnings

Sugargirl Glow Up Body Illuminator Shimmer Sunscreen SPF 30 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 10%, Octocrylene 6%, 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 doctor if

• rash occurs.

Keep out of reach of children.

• If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Apply generously and evenly 15 minutes before sun exposure.
• 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

MINERAL OIL (PARAFFINUM LIQUIDUM), HYDROGENATED STYRENE/ISOPRENE COPOLYMER, SILICA DIMETHYL SILYLATE, GLYCERYL CAPRYLATE, FRAGRANCE (PARFUM), SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL, SQUALANE, MACADAMIA INTEGRIFOLIA SEED OIL, OLEA EUROPAEA (OLIVE) FRUIT OIL, PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE, SYNTHETIC FLUORPHLOGOPITE, BENZYL ALCOHOL, COUMARIN, IRON OXIDES (CI 77491), MICA, TITANIUM DIOXIDE (CI 77891), TIN OXIDE, FD&C YELLOW NO. 5 (CI 19140), FD&C RED NO. 40 (CI 16035).

Questions or comments?

1-212-244-5170

Package Labeling:

INGREDIENTS AND APPEARANCE

SUGARGIRL GLOW UP BODY ILLUMINATOR SHIMMER SUNSCREEN SPF 30 
homosalate, octocrylene, octisalate, avobenzone gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85179-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	100 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	60 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
MINERAL OIL (UNII: T5L8T28FGP)
SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)
JOJOBA OIL (UNII: 724GKU717M)
SQUALANE (UNII: GW89575KF9)
MACADAMIA OIL (UNII: 515610SU8C)
OLIVE OIL (UNII: 6UYK2W1W1E)
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
BENZYL ALCOHOL (UNII: LKG8494WBH)
COUMARIN (UNII: A4VZ22K1WT)
FERRIC OXIDE RED (UNII: 1K09F3G675)
MICA (UNII: V8A1AW0880)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
STANNIC OXIDE (UNII: KM7N50LOS6)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C RED NO. 40 (UNII: WZB9127XOA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85179-002-00	100 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/02/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/02/2025

Labeler - I World LLC (830590126)