FDA.reportPublic FDA data

Sunglitter Princess

Manufacturer
Products On The Go, LLC
Effective date
2017-05-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:16:22

Label at a glance#

ProductSunglitter Princess
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE
Label structure6 sections

Indications and uses

Helps prevent sunburn. If used as directed with other sun protection measures (see directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Titanium dioxide 6%

Zinc Oxide 6%

OTC - PURPOSE SECTION

Sun Protection

Uses:

INDICATIONS & USAGE SECTION

  • Helps prevent sunburn.
  • If used as directed with other sun protection measures (see directions), decreases the risk of skin cancer and early skin aging caused by the sun.

WARNINGS:

WARNINGS SECTION

  • For external use only.

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 consult physician 

OTC - STOP USE SECTION

if irritation or rash develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If product is swallowed, get medical attention or contact poison control center immediately.

DIRECTION:

DOSAGE & ADMINISTRATION SECTION

  • Apply liberally 15-minutes before sun exposure.
  • Reapply
  • At least every two-hours.
  • Immediately after swimming, sweating or towel drying.
  • SUN PROTECTION MEASURES: Spending time in the sun increase your risk of skin cancer and early skin aging. To decrease this risk, regularly use sunscreen with broad spectrum protection and an SPF rating of 15 or higher, along with other sun protection measures including:
  • Limit time in the sun, especially between 10am and 2pm.
  • Wear long sleeve shirts, pants, hats and sunglasses.
  • For children under 6-months, consult a physician.

Other Ingredients:

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Camellia Sinensis (Green Tea) Extract, Cyanocobalamin (Vitamin B12), Daucus Carota Sativa (Carrot) Extract, Ethylhexylglycerin, Ethylhexyl Palmitate, Glycerin, Glycine Soja (Soybean) Oil, Helianthus Annuus (Sunflower) Extract, Lecithin, Parfum (Fragrance), Phenoxyethanol, Polyethylene Terephthalate (Glitter), Prunus Amygdalus Dulcis (Sweet Almond) Oil, Sesamum Indicum (Sesame) Oil, Sodium Laurylglucosides Hydroxypropylsulfonate Theobroma Cacao (Cocoa) Butter, Tocopherol (Vitamin E), Xanthan Gum.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130855997007156GTIN-13: 0855997007156
EAN-13: 0855997007156
GTIN-12: 855997007156
UPC-A: 855997007156
GTIN storage (14 digits): 00855997007156		Label.jpg

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70668-82670668-826-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
CYANOCOBALAMINP6YC3EG204IACT
CARROTL56Z1JK48BIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
ETHYLHEXYL PALMITATE2865993309IACT
GLYCERINPDC6A3C0OXIACT
SOYBEAN OIL241ATL177AIACT
HELIANTHUS ANNUUS FLOWERING TOPBKJ0J3D1BPIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ALMOND OIL66YXD4DKO9IACT
SESAME OILQX10HYY4QVIACT
COCOAD9108TZ9KGIACT
TOCOPHEROLR0ZB2556P8IACT
XANTHAN GUMTTV12P4NEEIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
ZINC OXIDESOI2LOH54ZACTIM

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
074bddcc-0579-384a-e063-6294a90a048f4fa81cb5-0d90-5a1e-e054-00144ff88e882023-10-09WarningsExact identifier
spl set id: 4fa81cb5-0d90-5a1e-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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