Sugargirl Glow Up Body Illuminator Shimmer Sunscreen SPF 30

Manufacturer
I World LLC
Effective date
2026-02-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:44:09

Label at a glance#

ProductSugargirl Glow Up Body Illuminator Shimmer Sunscreen SPF 30
Active ingredientHOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE
Label structure8 sections

Indications and uses

Helps prevent sunburn.

Dosage and administration

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.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Homosalate 10%, Octocrylene 6%, Octisalate 5%, Avobenzone 3%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

Helps prevent sunburn.

Warnings

WARNINGS SECTION

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

OTC - DO NOT USE SECTION

  • on damaged or broken skin.

When using this product

OTC - WHEN USING SECTION

  • Keep out of eyes. rinse with water to remove.

Stop use and ask doctor if

OTC - STOP USE SECTION

  • rash occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

SPL UNCLASSIFIED SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

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?

OTC - QUESTIONS SECTION

1-212-244-5170

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85179-002-00Sugargirl Glow Up Body Illuminator Shimmer Sunscreen SPF 30100 mL in 1 BOTTLE, PUMPGEL1002

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85179-00285179-002-00

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sugargirl Glow Up Body Illuminator Shimmer Sunscreen SPF 30HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONEI World LLC364d4d87-2d3e-4515-a3f2-1506d871699d2026-02-10WarningsExact identifier
ndc (package): 85179-002-00
ndc (product): 85179-002
ndc11 (package): 85179000200
spl id: 4a78c364-b895-3376-e063-6394a90ab095
spl set id: 364d4d87-2d3e-4515-a3f2-1506d871699d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.