Sugargirl SPF 30 Sunscreen Illuminating Stick Sunlight

Manufacturer
I World LLC
Effective date
2026-04-17
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:54:42

Label at a glance#

ProductSugargirl SPF 30 Sunscreen Illuminating Stick Sunlight
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 exposer. 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 15%, Octocrylene 8%, 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, notskin 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 a 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 centre right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

SPL UNCLASSIFIED SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

MICA, ISONONYL ISONONANOATE, SYNTHETIC WAX, ETHYLHEXYL PALMITATE, HYDROGENATED CASTOR OIL, SYNTHETIC FLUORPHLOGOPITE, BUTYLOCTYL SALICYLATE, DIISOSTEARYL MALATE, TAPIOCA STARCH, TRIETHOXYCAPRYLYLSILANE, GLYCERYL CAPRYLATE, POLYGLYCERYL-3 DIISOSTEARATE, CETYL PEG/PPG-10/1 DIMETHICONE, DIMETHICONE, POLYHYDROXYSTEARIC ACID, DISTEARDIMONIUM HECTORITE, SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, TRITICUM VULGARE (WHEAT) GERM OIL, PROPYLENE CARBONATE, STYRENE/BUTADIENE COPOLYMER, TITANIUM DIOXIDE(CI 77891), IRON OXIDES (CI 77492), IRON OXIDES (CI 77491), IRON OXIDES (CI 77499).

Questions or comments?

OTC - QUESTIONS SECTION

1-212-244-5170  info@amora.beauty

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle7Bottle7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85179-048-00Sugargirl SPF 30 Sunscreen Illuminating Stick Sunlight10 g in 1 TUBESTICK104

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85179-04885179-048-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-01-27monthly-update2026-06-03 17:56:22

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 SPF 30 Sunscreen Illuminating Stick SunlightHOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONEI World LLC28c9f019-34fe-4568-ba35-38eb3c4cb19e2026-04-17WarningsExact identifier
ndc (package): 85179-048-00
ndc (product): 85179-048
ndc11 (package): 85179004800
spl id: 4fab854a-c0ee-1f7b-e063-6394a90a75b1
spl set id: 28c9f019-34fe-4568-ba35-38eb3c4cb19e

Reported adverse events (FAERS/openFDA)#

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