LINO

Manufacturer
Lino Cosmetics LLC | Inspec Solutions LLC. | Inspec Solutions LLC
Effective date
2026-01-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:32:18

Label at a glance#

ProductLINO
Active ingredientZINC OXIDE
Label structure12 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.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 24.00%

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

Do not use on damaged or broken skin.

When using this product

OTC - WHEN USING SECTION

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

Stop use

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs.

Keep out of reach of children

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.

Direction

DOSAGE & ADMINISTRATION SECTION

Directions

Apply generously and evenly 15 minutes before sun exposure

Not suitable for children
apply to all skin exposed to the sun

Reapply

after 80 minutes of swimming or sweating
immediately after towel drying
at least every 2 hours

Apply using your hands, blending into the top half of your arm, then forearm, upper leg and then lower leg, ensuring you are covering all skin. Use more product if needed.

This product includes a gradual tan, therefore, please wash hands after use as product may stain.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf

Ascorbyl Tetraisopalmitate

Butyloctyl Salicylate

C13-15 Alkane

Caprylyl Glycol

Cetyl Diglyceryl Tris(Trimethylsiloxy)silylethyl Dimethicone

Dimethicone

Ethylhexylglycerin

Glycerin

Green Tea Extract

Isopropyl Myristate

Niacinamide

Pentylene Glycol

Phenoxyethanol

Polyhydroxystearic acid

Propanediol

Silica

Sodium Chloride

Sodium Phytate

Sorbitan Olivate

Synthetic Beeswax

Water

Questions?

OTC - QUESTIONS SECTION

Call toll free 1-888-942-2887

LINO SPF 50

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LINOLINO

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130198715428216GTIN-13: 0198715428216
EAN-13: 0198715428216
GTIN-12: 198715428216
UPC-A: 198715428216
GTIN storage (14 digits): 00198715428216
LINO SPF 50.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84749-001-01LINO30 g in 1 BOTTLE, PLASTICCREAM302

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84749-00184749-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 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
LINOZINC OXIDELino Cosmetics LLC262ef129-9453-2411-e063-6294a90ae2232026-01-12WarningsExact identifier
ndc (package): 84749-001-01
ndc (product): 84749-001
ndc11 (package): 84749000101
spl id: 483298d5-3d0e-7dfe-e063-6294a90a05bf
spl set id: 262ef129-9453-2411-e063-6294a90ae223

Reported adverse events (FAERS/openFDA)#

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