NATURAL SUNSCREEN

Manufacturer
HUSH BRANDS INC. | Empack Spraytech Inc.
Effective date
2019-04-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:19:38

Label at a glance#

ProductNATURAL SUNSCREEN SPF 40
Active ingredientZINC OXIDE
Label structure9 sections

Dosage and administration

Apply liberally and generously 15 minutes before sun exposure. • reapply: • after 40 minutes of swimming or sweating • immediately after towel drying • at least every 2 hours. 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 inc...

Label contents#

Full prescribing information#

Active Ingredients (w/w )/ Ingrédients actifs (p/p)

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 20.5%

Purpose/ Utilité

OTC - PURPOSE SECTION

Sunscreen/ Écran solaire

Use/ Usage

INDICATIONS & USAGE SECTION

Helps prevent sunburn/ Aide à prévenir les coups de soleil

Warnings / Mises en garde

WARNINGS SECTION

For external use only/ Pour usage externe seulement

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin/ Ne pas utiliser sur la peau endommagée ou présentant des lesions 

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs/ Cesser d’utiliser ce produit et consultez un médecin si une éruption cutanée apparait

OTC - WHEN USING SECTION

When using this product keep out of eyes. Rinse with water to remove/ Lorsque vous utilisez ce produit éviter tout contact avec les yeux. Rincer à l’eau le cas échéant.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.Store at room temperature 15-30°C (59-86°F)/ Garder hors de la portée des enfants. Topique. En cas d’ingestion, consulter un médecin immédiatement ou appeler un centre antipoison. Conserver à la température de la pièce entre 15-30°C (59-86°F)

Directions / Mode d’emploi

DOSAGE & ADMINISTRATION SECTION

  • Apply liberally and generously 15 minutes before sun exposure. • reapply: • after 40 minutes of swimming or sweating
    • immediately after towel drying • at least every 2 hours. 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 am - 2 pm • wear long-sleeved shirts, pants, hats, and sunglasses. • For use on children less than 6 months of age, consult a doctor

Appliquer abondamment et généreusement 15 minutes avant l’exposition au soleil • Appliquer de nouveau : • après 40 minutes de baignade ou après avoir transpire • immédiatement après s’être séché à la serviette • au moins toutes les 2 heures. Mesures de protection contre le soleil : Passer du temps au soleil augmente le risque de cancer de la peau et de vieillissement prématuré de la peau. Afin de diminuer ce risque, il convient d’utiliser régulièrement un écran solaire avec un F.P.S. à large spectre d’au moins 15 et d’appliquer d’autres mesures de protection contre le soleil, telles que : • limiter le temps passé au soleil, notamment entre 10 et 14 heures • porter des chemises à manches longues, des pantalons, un chapeau et des lunettes de soleil • Pour les enfants âgés de moins de 6 mois, consulter un médecin.

Other Information / Autres renseignements

OTHER SAFETY INFORMATION

  • Protect the product in this container from excessive heat and direct sun. May stain surfaces and fabrics/ Tenir loin de la chaleur excessive ou des rayons de soleil. Peut tacher certains tissus et surfaces.

Inactive Ingredients / Ingrédients inactifs

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Ammonium Acryloyldimethyltaurate / VP Copolymer, Aqua/Water/Eau, Bambusa Arundinacea Stem Extract, Camellia Sinensis Leaf Extract, Caprylic/Capric Triglycerides, Dilauryl Citrate, Ethylhexylglycerin, Ginkgo Biloba Leaf Extract, Gluconolactone, Glycine Soja (Soybean) Oil, Glycerin, Hydrogenated Methyl Abietate, Isopropyl Palmitate, Lauryl Glucoside, Leuconostoc/Radish Root Ferment Filtrate, Lonicera Caprifolium (Honeysuckle) Flower Extract, Lonicera Japonica (Honeysuckle) Flower Extract, Methylcellulose, Octyldodecyl Citrate Crosspolymer, Phenoxyethanol, Polyglyceryl-4 Laurate, Polyhydroxystearic Acid, Populus Tremuloides Bark Extract, Simmondsia Chinensis (Jojoba) Seed Oil, Sodium Lauryl Glucose Carboxylate, Sodium Phytate, Sodium Stearoyl Glutamate, Sorbitan Laurate, Tocopherol, Xanthan Gum.

Questions?

OTC - QUESTIONS SECTION

1-866-923-2665

Manufactured in Canada by/ Fabriqué au Canada par: Empack Spraytech Inc., 98 Walker Drive, Brampton, ON, L6T 4H6

UPC Please recycle (+ logo) Lot # and Expiry Date to be embossed on the tube seal

Principal Display Panel - NATURAL SUNSCREEN LOTION SPF/FPS 40 ÉCRAN SOLAIRE NATUREL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NATURAL SUNSCREEN LOTION

SPF/FPS 40

ÉCRAN SOLAIRE NATUREL

BROAD SPECTRUM SPF/FPS 40 À LARGE SPECTRE   

UVA/UVB PROTECTION

Water/ Sweat Resistant (40 MINUTES)/ Résistant à l'eau/résistant à la transpiration (40 minutes)

Non-whitening. Fast absorbing. Unscented/ non-blanchissant. Absorption rapide. Non parfumé

3.4 fl. oz. /100 ml

Principal Display Panel - NATURAL SUNSCREEN LOTION SPF 40 TubePrincipal Display Panel - NATURAL SUNSCREEN LOTION SPF 40 Tube

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73022-004-012024-01-30C16284748780-11030e365-50e1-111a-e063-dadaa90a10e2Drug Facts

Products#

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

DailyMed product names page 1 of 1 · 33 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73022-00473022-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 32 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
e8900f69-b6eb-4eb9-a18c-c34095a1090d6bb1814e-07f5-4a8d-9249-71f19358b8fe2019-04-12WarningsExact identifier
spl id: e8900f69-b6eb-4eb9-a18c-c34095a1090d
spl set id: 6bb1814e-07f5-4a8d-9249-71f19358b8fe

Reported adverse events (FAERS/openFDA)#

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