HWT SPF 30 Unscented Face Sunscreen 2fl oz

Manufacturer
Naturich Labs, Inc
Effective date
2021-01-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:36:28

Label at a glance#

ProductHWT SPF 30 Unscented Face Sunscreen 2fl oz
Active ingredientZINC OXIDE
Label structure12 sections

Dosage and administration

Apply generously 15 minutes before sun exposure. For children under 6 months of age; Ask a doctor Reapply at least every 2 hours Use water-resistant sunscreen if swimming or sweating Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measu...

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide: 11.25% Purpose: Sunscreen

Titanium Dioxide: 1.50% Purpose: Sunscreen

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

OTC - WHEN USING SECTION

When using this product, keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition. Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

Use

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 on damage or broken skin.

When using this product, keep out of eyes. Rinse with water to remove

Stop use and ask a doctor if rash occurs.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Do not use

OTC - DO NOT USE SECTION

In children less than 2 months of age.

On open skin wounds

Stop use and contact a doctor if rash occurs.

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. Theses may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help of contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply generously 15 minutes before sun exposure.

For children under 6 months of age; Ask a doctor

Reapply at least every 2 hours

Use water-resistant sunscreen if swimming or sweating

Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including limit time in the sun, especially from 10 a.m. -2 p.m, and wear long-sleeved shirts, pants, hats, and sunglasses.

Additional Information

STORAGE AND HANDLING SECTION

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

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water (Aqua), Organic Aloe Barbadensis Leaf Juice, Caprylic/Capric Triglyceride, Glycerin, Cetearyl Alcohol, Coconut Alkanes, Coco-Caprylate, Cetearyl Glucoside, Cetyl Palmitate, Galactoarabinan, Rosa Centifolia Flower Extract, Lavandula Angustifolia (Lavender) Flower Extract, Camellia Sinensis (Green Tea) Leaf Extract, Sorbitan Oleate, Sorbitan Palmitate, Anhydroxylitol, Coco-Caprylate/Caprate, Xylitylglucoside, Xylitol, Glyceryl Isostearate, Polyhydroxystearic Acid, Tocopherol, Sorbitan Isostearate, Caprylyl/Capryl Glucoside, Hydroxyethyl Acrylate/ Sodium Acryloyldimethyl Taurate Copolymer, Alumina, Jojoba Esters, Phenoxyethanol, Benzyl Alcohol.

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SPF Tube FrontSPF Tube Front

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72496-1055-22023-01-30C16284748780-1f386c64a-4722-0266-e053-dadaa90a7c1aHawthorne Face Sunscreen SPF 30

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72496-1055-2HWT SPF 30 Unscented Face Sunscreen 2fl oz60 g in 1 TUBECREAM602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72496-1055HWT SPF 30 UNSCENTED FACE SUNSCREEN 2FL OZ (HAWTHORNE FACE SUNSCREEN SPF 30) CREAM [NATURICH LABS, INC]2Legacy NDC, 1 package rows20210106_b82da458-a073-6223-e053-2a95a90acbcf.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72496-105572496-1055-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ZINC OXIDESOI2LOH54ZACTIB

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
b82eb604-a3dd-5fd3-e053-2995a90a00c2b82da458-a073-6223-e053-2a95a90acbcf2021-01-05WarningsExact identifier
spl id: b82eb604-a3dd-5fd3-e053-2995a90a00c2
spl set id: b82da458-a073-6223-e053-2a95a90acbcf

Reported adverse events (FAERS/openFDA)#

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