OI LIN DEEP MOISTURE SUNSCREEN SPF 25 Tinted

Manufacturer
Sunrider Manufacturing L.P.
Effective date
2019-12-18
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 23:50:14

Label at a glance#

ProductOI LIN DEEP MOISTURE SUNSCREEN SPF 25 Tinted
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE
Label structure7 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

USES:  HELPS PREVENT SUNBURNS

DOSAGE & ADMINISTRATION SECTION

RECOMMENDATION:  APPLY GENEROUSLY TO FACE BEFORE EXPOSURE TO SUN, AVOIDING CONTACT WITH EYES. REAPPLY TO EXPOSED AREAS AS NEEDED THROUGHOUT THE DAY.

OTC - ASK DOCTOR SECTION

CHILDREN UNDER 6 MONTHS OF AGE:  CONSULT A DOCTOR BEFORE USE.

WARNINGS SECTION

WARNING:  FOR EXTERNAL USE ONLY, IF SWALLOWED, SEEK MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.  IF CONTACT WITH EYES OCCURS, RINSE THOROUGHLY WITH WATER.  DISCONTINUE USE AND CONSULT A DOCTOR IF PERSISTENT SIGNS OF IRRITATION OR RASH APPEAR.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS:

TITANIUM DIOXIDE 9.4%

ZINC OXIDE 3.9%

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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

DailyMed product names page 1 of 2 · 53 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62191-03262191-032-05

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 51 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
94cf656b-9702-4f1e-b9a5-78b55f073c063048324a-ab41-41d2-a6e5-7c4354f37fa62019-12-18WarningsExact identifier
spl id: 94cf656b-9702-4f1e-b9a5-78b55f073c06
spl set id: 3048324a-ab41-41d2-a6e5-7c4354f37fa6

Reported adverse events (FAERS/openFDA)#

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