FDA.reportPublic FDA data

Crunchi Sunlight SPF 30 Daily Facial Lotion

Manufacturer
Bell International Laboratories, Inc
Effective date
2023-03-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:35:00

Label at a glance#

ProductSunlight Daily Facial SPF 30
Active ingredientZINC OXIDE
Label structure8 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

Apply liberally 15 minutes before sun exposure. Children under 6 months of age: ask a doctor. Reapply at least every 2 hours. Reapply after swimming or sweating. Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrase this risk, regularly use a sunscreen with a Broad Spectrum value of 15 or higher and other sun protection measures including: Limit time ...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 12.5%

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

Warnings

WARNINGS SECTION

For external use only.

Do not use on damaged 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.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply liberally 15 minutes before sun exposure. Children under 6 months of age: ask a doctor. Reapply at least every 2 hours. Reapply after swimming or sweating. Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrase this risk, regularly use a sunscreen with a Broad Spectrum value of 15 or higher and other sun protection measures including:

  • Limit time in the sun, especially from 10 a.m. to 2 p.m.
  • wear long-sleeved shirts, pants, hats, and sunglasses
  • Use a water resistant sunscreen if swimming or sweating.

Other Informaiton

OTHER SAFETY INFORMATION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Bisabolol, Butyloctyl Salicylate, Butyrospermum Parkii (Shea) Butter, Cetearyl Alcohol, Cetearyl Olivate, Cetyl Palmitate, Citric Acid, Coco-Caprylate/Caprate, Coconut Alkanes, Ethyl Ferulate, Ethylhexyl Olivate, Glyceryl Caprylate, Glyceryl Undecylenate, Heptyl Undecylenate, Phenothyl Alcohol. Polyhydroxstearic Acid, Propanediol, Sodium Hyaluronate, Sodium Phytate, Sodium Stearoyl Glutamate, Sorbitan Oleate, Sorbitan Olivate, Sorbitan Palmitate, Squalene, Tocopherol, Triethoxycaprylylsilane, Vitis Vinifera (Grape) Seed Oil, Water, Xanthan Gum

Labels

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

bottlebottleboxbox

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76150-293-342023-03-06C16284748780-1f386c64a-29d3-0266-e053-dadaa90a7c1aCrunchi Sunlight SPF 30 Daily Facial Lotion
76150-293-342023-01-30C16284748780-1f386c64a-29d3-0266-e053-dadaa90a7c1aCrunchi Sunlight SPF 30 Daily Facial Lotion

Products#

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

DailyMed product names page 1 of 1 · 30 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76150-29376150-293-34

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

Name, UNII, Kind table
NameUNIIKind
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
GLYCERYL CAPRYLATETM2TZD4G4AIACT
XANTHAN GUMTTV12P4NEEIACT
TOCOPHEROLR0ZB2556P8IACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
GLYCERYL 1-UNDECYLENATEB68LJT9544IACT
HYALURONATE SODIUMYSE9PPT4THIACT
ETHYL FERULATE5B8915UELWIACT
CETEARYL OLIVATE58B69Q84JOIACT
COCO-CAPRYLATE/CAPRATE8D9H4QU99HIACT
PHENYLETHYL ALCOHOLML9LGA7468IACT
WATER059QF0KO0RIACT
SODIUM STEAROYL GLUTAMATE65A9F4P024IACT
LEVOMENOL24WE03BX2TIACT
PHYTATE SODIUM88496G1ERLIACT
HEPTYL UNDECYLENATEW77QUB6GXOIACT
ZINC OXIDESOI2LOH54ZACTIB
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
PROPANEDIOL5965N8W85TIACT
SQUALANEGW89575KF9IACT
SORBITAN MONOPALMITATE77K6Z421KUIACT
COCONUT ALKANES1E5KJY107TIACT
CETYL PALMITATE5ZA2S6B08XIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
GRAPE SEED OIL930MLC8XGGIACT
ETHYLHEXYL OLEATER34927QY59IACT
SHEA BUTTERK49155WL9YIACT

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
f6440282-4633-f9d2-e053-2995a90afbe2bff108d1-de6f-6d4a-e053-2995a90a69372023-03-06WarningsExact identifier
spl id: f6440282-4633-f9d2-e053-2995a90afbe2
spl set id: bff108d1-de6f-6d4a-e053-2995a90a6937

Reported adverse events (FAERS/openFDA)#

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