Facial Sunscreen with Zinc SPF 50

Manufacturer
Rite Aid | Product Quest Mfg
Effective date
2018-05-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:55:30

Label at a glance#

ProductFacial Sunscreen with Zinc SPF 50 Daylogic
Active ingredientOctinoxate, Octisalate, Oxybenzone, Zinc Oxide
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients                                                                     Purpose
Octinoxate 7.5%.......................................................................Sunscreen
Octisalate 5.0%........................................................................Sunscreen
Oxybenzone 6.0%...................................................................Sunscreen
Zinc Oxide 7.0%.......................................................................Sunscreen

INDICATIONS & USAGE SECTION

Uses • helps prevent sunburn

WARNINGS SECTION

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

DOSAGE & ADMINISTRATION SECTION

Directions
• apply liberally 15 minutes before sun exposure
• 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 this risk, regularly
use a sunscreen with a broad spectrum SPF of 15 or higher and other
sun protection measures including:
• limit time in the sun, especially from 10 a.m. – 2 p.m.
• wear long-sleeve shirts, pants, hats, and sunglasses
• children under 6 months: Ask a doctor

OTHER SAFETY INFORMATION

Other information
• protect this product from excessive heat and direct sun.

INACTIVE INGREDIENT SECTION

Inactive ingredients

Aloe Barbadensis Leaf Extract,
Beeswax, Cetyl Dimethicone, Cetyl PEG/PPG-10/1 Dimethicone,
Cyclopentasiloxane, Cyclohexasiloxane, Diisopropyl Adipate, DMDM
Hydantoin, Ethylhexyl Palmitate, Ethylhexyl Stearate, Glycerin, Hydrated
Silica, Hydrogenated Castor Oil, Polyethylene, Sodium Chloride,
Theobroma Cacao (Cocoa) Seed Butter, Tocopheryl Acetate,
Triethoxycaprylylsilane, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11822-1214-12020-01-31C16284748780-19d75b9d0-243d-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11822-1214-1Facial Sunscreen with Zinc SPF 50Daylogic28.3 g in 1 JARCREAM28.31

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-1214FACIAL SUNSCREEN WITH ZINC SPF 50 DAYLOGIC (OCTINOXATE 7.50% OCTISALATE 5.00% OXYBENZONE 6.00% ZINC OXIDE 7.00%) CREAM [RITE AID]1Legacy NDC, 1 package rows20180512_8fb6968e-c70a-4f6d-8558-7882d48c511e.zip

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11822-121411822-1214-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Source Document#

Source XML · Source PDF

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
8fc8d766-40e6-4423-b786-3d124309ff2f8fb6968e-c70a-4f6d-8558-7882d48c511e2018-05-11WarningsExact identifier
spl id: 8fc8d766-40e6-4423-b786-3d124309ff2f
spl set id: 8fb6968e-c70a-4f6d-8558-7882d48c511e

Reported adverse events (FAERS/openFDA)#

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