FDA.reportPublic FDA data

Unicorn Snot SPF 30 Bioglitter Sunscreen

Manufacturer
Jaibreak Toys, Inc
Effective date
2022-12-07
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
legacy-cache
Hydrated at
2026-08-01 21:45:11

Label at a glance#

ProductUnicorn Snot SPF 30 Bioglitter Sunscreen
Active ingredientOCTINOXATE, OCTOCRYLENE, HOMOSALATE, AVOBENZONE
Label structure7 sections

Dosage and administration

• Apply liberally and evenly 15 minutes before sun exposure. • Reapply: At least every two hours. Immediately after swimming, sweating or towel drying. For children under 6 months, consult a physician.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Octinoxate 7%, Octocrylene 7%,
Homosalate 5%, Avobenzone 2.5%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

INDICATIONS & USAGE SECTION

Helps prevent sunburn.

Warnings

WARNINGS SECTION

• For external use only

Do not use

OTC - DO NOT USE SECTION

on damaged or broken skin

Stop use and ask doctor

OTC - STOP USE SECTION

  • if rash occurs.

When using this product

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

• Apply liberally and evenly 15 minutes before sun exposure. • Reapply: At least every two hours. Immediately after swimming, sweating or towel drying. For children under 6 months, consult a physician.

Other information

SPL UNCLASSIFIED SECTION

Protect this product from excessive heat and direct sunlight.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua (Deionized Water), Beeswax, Butyloctyl Salicylate, Caprylic/Capric Triglyceride, Disodium EDTA, Glitter (Polylactide, Polybutylene Terephthalate), Glyceryl Stearate, Hyaluronic Acid, Isopropyl Myristate, Parfum (Fragrance), PEG-100 Stearate, Potassium Sorbate, Sodium Benzoate, Steareth-2, Steareth-20, Tapioca Starch, VP/Eicosene Copolymer, Xanthan Gum

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72192-94272192-942-05

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
YELLOW WAX2ZA36H0S2VIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
POLYLACTIDE459TN2L5F5IACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
HYALURONIC ACIDS270N0TRQYIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
PEG-100 STEARATEYD01N1999RIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
SODIUM BENZOATEOJ245FE5EUIACT
STEARETH-2V56DFE46J5IACT
STEARETH-20L0Q8IK9E08IACT
STARCH, TAPIOCA24SC3U704IIACT
XANTHAN GUMTTV12P4NEEIACT
OCTINOXATE4Y5P7MUD51ACTIB
OCTOCRYLENE5A68WGF6WMACTIB
HOMOSALATEV06SV4M95SACTIB
AVOBENZONEG63QQF2NOXACTIB

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
074c14dd-367b-98e1-e063-6294a90ada9ae4b1960e-6f0b-4db3-b001-76028898ee922023-10-09WarningsExact identifier
spl set id: e4b1960e-6f0b-4db3-b001-76028898ee92

Reported adverse events (FAERS/openFDA)#

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