MUGWORT SUNSCREEN

Manufacturer
Dongguan Haiyi Technology Co.,Ltd.
Effective date
2024-09-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:22:01

Label at a glance#

ProductMUGWORT SUNSCREEN
Active ingredientWATER
Label structure10 sections

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Water

Inactive ingredient

INACTIVE INGREDIENT SECTION

Zinc Oxide,Cycohexasiloxane, Butylocty Salicylate,Propanediol, Propyheptyl Caprylate, lsododecane, Polyglycery1-3Polydimethylsiloxyethyl Dimethicone, Caprylyl Methicone, DicaprylyCarbonate, Methyl Methacrylate Crosspolymer, Polymethylsilsesqui-oxane, Centella Asiatica Extract, Artemisia Capilaris Extract,Houttuyia Cordata Extract, Melaleuca Alterifolia (Tea Tree) Extract,Sodium Hyaluronate, Disteardimonium Hectorite, MagnesiumSulfate, Triethoxycaprylylsilane,1,2-hexanediol, Polyglycery1-2Dipolyhydroxystearate, Laury! Polyglycery!-3 Polydimethylsiloxyeth-y Dimethicone, Phenyl Trimethicone, Acrylates/dimethiconeCopolymer, Glyceryl Caprylate, Caprylyl Glycol, Ethylhexylglycerin,Tocopherol, Butylene Glycol, Pentylene Glycol

Purpose section

OTC - PURPOSE SECTION

A physical sun cream features a broad spectrum ofSPF 50+ PA++++ that protects the skin fom UV rays.Fomulated with Centella Asiatica Extract, Houttuynia CordataExtract, Tea Tree Extract and Artemisia Capillaris Exract that helpsoothe sensitive and irritated skin.The physical formula helps for a skin protection barier to reflectand block the UV rays.
The watery cream texture keeps the skin refreshing and molsturizedunder the sunlight without white cast.

Warning

WARNINGS SECTION

For external use onlyWhen using this product keep out ofeyesRinse with water to remove.Stop use and ask a doctor if rashoccurs.Keep out of reach of children. Do not use ondamaged ordiseased skin. For sensitive skins,test product for any skin irritationon a smallarea of the skin prior to use. lf accidentalingestionoccurs please contact a PoisonControl Center right away. Consulta doctorbefore use on children under 6 months of age.

stop use

OTC - STOP USE SECTION

This product may cause allergic reactions in asmall number of people.
lf youexperience any discomfort,please stop using it immediately.

not use

OTC - DO NOT USE SECTION

Not suitable for use by children, pregnantor breastfeeding people.

OUT OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP THE PRODUCT OUT OF REACH OF CHILDREN to

HOW TO USE

INDICATIONS & USAGE SECTION

1. Apply it at the last stage of skincare routine 15 minutesbefore heading out.
2. Apply an approximate size of a finger twice to threetimes.
3. The soft and moisturizing texture allows you to apply atany time.

Dosage

DOSAGE & ADMINISTRATION SECTION

take an appropriateamount,Use 2-3 times a week

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84732-017-012025-07-29C16284748780-13b156c62-2bdb-fb37-e063-e6dba90a4e0723019c89-6d85-6319-e063-6394a90ab092

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84732-017-01MUGWORT SUNSCREEN50 mL in 1 BOTTLE, PLASTICCREAM501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84732-017MUGWORT SUNSCREEN CREAM [DONGGUAN HAIYI TECHNOLOGY CO.,LTD.]11 package rows20240927_23019c89-6d85-6319-e063-6394a90ab092.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84732-01784732-017-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
23019c89-6d86-6319-e063-6394a90ab09223019c89-6d85-6319-e063-6394a90ab0922024-09-26WarningsExact identifier
spl id: 23019c89-6d86-6319-e063-6394a90ab092
spl set id: 23019c89-6d85-6319-e063-6394a90ab092

Reported adverse events (FAERS/openFDA)#

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