FDA.reportPublic FDA data

Crunchi Sunlight Daily Facial Sunscreen SPF 30

Manufacturer
Cruchi, LLC.
Effective date
2025-12-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:23:37

Label at a glance#

ProductCrunchi Sunlight Daily Facial Sunscreen 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. Re-apply 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 decrease the risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: Limit ...

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

OTC - DO NOT USE SECTION

on damaged or broken skin.

•  When using this product

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

•  Stop use and ask a doctor

OTC - STOP USE SECTION

if rash occurs.

•  Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • 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. Re-apply at least every 2 hours. Reapply after swimming or sweating.  Sun Protection MeasuresSpending 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 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 Information

SPL UNCLASSIFIED SECTION

  • 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, Phenethyl Alcohol, Polyhydroxystearic Acid, Propanediol, Sodium Hyaluronate, Sodium Phytate, Sodium Stearoyl Glutamate, Sorbitan Oleate, Sorbitan Olivate, Sorbitan Palmitate, Squalane, Tocopherol, Triethoxycaprylylsilane, Vitis Vinifera (Grape) Seed Oil*, Water, Xanthan Gum

*Certified Organic Ingredients

Questions or comments?

OTC - QUESTIONS SECTION

www.crunchi.com (888) 831-3133

Package Labelling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label01.jpgLabel01.jpgLabel02.jpgLabel02.jpg

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ZINC CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72444-0200-0Crunchi Sunlight Daily Facial Sunscreen SPF 3030 mL in 1 BOTTLE, GLASSLIQUID302
72444-0200-0Crunchi Sunlight Daily Facial Sunscreen SPF 301 in 1 CARTONLIQUID12

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
72444-020072444-0200-0

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
LEVOMENOL24WE03BX2TIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
SHEA BUTTERK49155WL9YIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
CETEARYL OLIVATE58B69Q84JOIACT
CETYL PALMITATE5ZA2S6B08XIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
COCOYL CAPRYLOCAPRATE8D9H4QU99HIACT
COCONUT ALKANES1E5KJY107TIACT
ETHYL FERULATE5B8915UELWIACT
ETHYLHEXYL OLIVATEHTC7G3S2PVIACT
GLYCERYL CAPRYLATETM2TZD4G4AIACT
HEPTYL UNDECYLENATEW77QUB6GXOIACT
PHENYLETHYL ALCOHOLML9LGA7468IACT
PROPANEDIOL5965N8W85TIACT
HYALURONATE SODIUMYSE9PPT4THIACT
PHYTATE SODIUM88496G1ERLIACT
SODIUM STEAROYL GLUTAMATE65A9F4P024IACT
SORBITAN MONOOLEATE06XEA2VD56IACT
SORBITAN OLIVATEMDL271E3GRIACT
SORBITAN MONOPALMITATE77K6Z421KUIACT
SQUALANEGW89575KF9IACT
TOCOPHEROLR0ZB2556P8IACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
GRAPE SEED OIL930MLC8XGGIACT
WATER059QF0KO0RIACT
XANTHAN GUMTTV12P4NEEIACT
ZINC OXIDESOI2LOH54ZACTIM

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
Crunchi Sunlight Daily Facial Sunscreen SPF 30ZINC OXIDECruchi, LLC.4f3bcfa0-e43e-4284-afaa-6488ddd749f02025-12-15WarningsExact identifier
ndc (package): 72444-0200-0
ndc (product): 72444-0200
ndc11 (package): 72444020000
spl id: 45ff6623-d2bd-8bd1-e063-6394a90a8091
spl set id: 4f3bcfa0-e43e-4284-afaa-6488ddd749f0

Reported adverse events (FAERS/openFDA)#

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