FDA.reportPublic FDA data

HEY HOTTIE Shimmer DRY OIL MIST SUNSCREEN SPF30

Manufacturer
Guangdong Aimu Biological Technology Co., Ltd
Effective date
2026-06-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-06-13 05:10:11

Label at a glance#

ProductHEY HOTTIE Shimmer dry oil mist sunscreen spf30
Active ingredientOCTINOXATE, OCTOCRYLENE
Label structure11 sections

Indications and uses

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

Dosage and administration

*Shake well and spray directly onto skin evenly 15 minutes before sun exposure. *Reapply at least every 2 hours use a water resistant sunscreen if swimming or sweating. *Sun Protection Measures: Spending time in the sun increases your risk of skin cancer andearly skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPFvalue of 15 or higher and other sun protection measures including: ...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

OCTOCRYLENE 2 %

OCTINOXATE 7.5%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

Helps prevent sunburn.

If used as directed with other sun protection measures (see Directions) decreases the risk ofskin cancer and early skin aging caused by the sun.

Warnings

WARNINGS SECTION

For external use only.

Stop use and ask a doctor if

OTC - STOP USE SECTION

rash occurs.

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.

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

*Shake well and spray directly onto skin evenly 15 minutes before sun exposure.

*Reapply at least every 2 hours use a water resistant sunscreen if swimming or sweating.

*Sun Protection Measures: Spending time in the sun increases your risk of skin cancer andearly skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPFvalue of 15 or higher and other sun protection measures including:

-limit time in the sun, especially from 10 a.m.

-2 p.m.wear long-sleeved shirts, pants, hats, and sunglasses.

*Children under 6 months of age: Ask a doctor.

Inactive ingredients

INACTIVE INGREDIENT SECTION

ALCOHOL,SIMMONDSIACHINENSIS(JOJOBA)SEEDOIL,POLYMETHYLSILSESQUIOXANE,CYCLOPENTASILOXANE,PARFUM,BISABOLOL,CI 77491

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label.Label.

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeCode 1286664465900.jpg

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83566-61383566-613-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
BISABOLOL24WE03BX2TIACT
CYCLOPENTASILOXANE0THT5PCI0RIACT
SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL724GKU717MIACT
CI 774911K09F3G675IACT
OCTINOXATE4Y5P7MUD51ACTIB
OCTOCRYLENE5A68WGF6WMACTIB
ALCOHOL3K9958V90MIACT
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS)59Z907ZB69IACT

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
HEY HOTTIE Shimmer dry oil mist sunscreen spf30OCTOCRYLENE,OCTINOXATEGuangdong Aimu Biological Technology Co., Ltd53f19c01-0011-bc70-e063-6294a90ab8792026-06-10WarningsExact identifier
ndc (package): 83566-613-01
ndc (product): 83566-613
ndc11 (package): 83566061301
spl id: 53f19c01-0012-bc70-e063-6294a90ab879
spl set id: 53f19c01-0011-bc70-e063-6294a90ab879

Reported adverse events (FAERS/openFDA)#

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