Chantecaille

Manufacturer
Bell International Laboratories, Inc
Effective date
2021-11-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:25:57

Label at a glance#

ProductChantecaille SPF 30
Active ingredientZINC OXIDE
Label structure9 sections

Indications and uses

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.

Dosage and administration

Hold container 4 to 6 inches from the skin to apply Spay liberally and spread evenly by hand 15 minutes before sun exposure Do not spray directly into face. Spray on hands then apply to face Do not apply in windy conditions Use in a well-ventilated areas Reapply: -After 80 minutes of swimming or sweating -Immediately after towel drying -At least every 2 hours Sun Protection Measures: Spending time in the sun incre...

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide - 15.2%

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 of skin cancer and early skin aging caused by the sun.

Warnings

WARNINGS SECTION

For external use only.

Contents under pressure. Do not puncture or incinerate.

Do note store at temperatures above 120 F.

Do not use on damaged or broken skin.

Stop use and ask a doctor if rash occurs.

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

Keep out of reach of children.

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

Directions

DOSAGE & ADMINISTRATION SECTION

Hold container 4 to 6 inches from the skin to apply

Spay liberally and spread evenly by hand 15 minutes before sun exposure

Do not spray directly into face. Spray on hands then apply to face

Do not apply in windy conditions

Use in a well-ventilated areas

Reapply:

-After 80 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 the risk, regularly use a sunscreen with a broad-spectrum SPF of 15 or higher and other protection measures including:

-Limit time in the sun, especially from 10 a.m. – 2 p.m.

-Wear long sleeves shirts, pants, hats, and sunglasses.

Children under 6 months: ask a doctor.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Citrus Aurantium Dulcis (Orange) Fruit Water, Water, Simmondsia Chinensis (Jojoba) Seed Oil, Butyloctyl Salicylate, Cocos Nucifera (Coconut) Oil, Methyl Dihydroabietate, Glycerin, Cetearyl Alcohol, Coco-Glucoside, Bentonite, Shea Butter Ethyl Esters, Aloe Barbadensis Leaf Juice, Helianthus Annuus (Sunflower) Seed Oil, Rubus Idaeus (Raspberry) Seed Oil, Rosmarinus Officinalis (Rosemary) Leaf Extract, Portulaca Oleracea Extract, Withania Somnifera Root Extract, Camellia Sinensis Leaf Extract, Fructose, Bisabolol, Ethyl Ferulate, Microcrystalline Cellulose, Cellulose Gum, Sodium Stearoyl Glutamate, Sodium Gluconate, Citric Acid, Caprylhydroxamic Acid, Caprylyl Glycol, Capryloyl Glycerin/Sebacic Acid Copolymer, Citrus Nobilis (Mandarin Orange) Peel Oil

Other Information

OTHER SAFETY INFORMATION

Protect this product from excessive heat and direct sun

Questions

OTC - QUESTIONS SECTION

To report a serious adverse event contact Chantecaille Beaute, Inc. 584 Broadway No. 1111 New York NY 10012

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SeaScreen SPF 30 LabelSeaScreen SPF 30 Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76150-328-132023-01-30C16284748780-1f386c649-fa40-0266-e053-dadaa90a7c1aSeaScreen 30 Mineral Broad-Spectrum Sunscreen Mist SPF 30

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
76150-32876150-328-13

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 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
d18b4daa-46ae-6aee-e053-2a95a90a0cdad162f560-12be-0d6c-e053-2995a90acaee2021-11-24WarningsExact identifier
spl id: d18b4daa-46ae-6aee-e053-2a95a90a0cda
spl set id: d162f560-12be-0d6c-e053-2995a90acaee

Reported adverse events (FAERS/openFDA)#

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