Sawyer SPF30 Lotion bottle (IS0358)

Manufacturer
Sawyer Products Inc | Inspec Solution
Effective date
2026-03-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:51:52

Label at a glance#

ProductStay Put Sunscreen SPF 30
Active ingredientOCTINOXATE, OCTISALATE, OXYBENZONE, HOMOSALATE
Label structure7 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 to cool, dry skin 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 includ...

Label contents#

Full prescribing information#

Actives                     Purpose

OTC - ACTIVE INGREDIENT SECTION

Octinoxate 7.50%       Sunscreen
Octisalate 5.00%        Sunscreen
Oxybenzone 4.00%    Sunscreen
Homosalate 10.00%   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

Directions

DOSAGE & ADMINISTRATION SECTION

apply liberally to cool, dry skin
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 a long-sleeve shirts,
pants, hats, and sunglasses. • children under 6
months: Ask a doctor

Warnings For external use only.

WARNINGS SECTION

Do not useon damaged or broken skin.
When using this product■ keep out of eyes. Rinse eyes with water
to remove.
Stop use and ask a doctor ifrash occurs

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if swallowed, get medical help or contact a Polson Control Center right away.

Inactive ingredeints

INACTIVE INGREDIENT SECTION

Purified Water
Hydrogenated Polyisobutene
Stearic Acid
Cetyl Alcohol
Amphisol (DEA-cetyl phosphate)
Glydant Plus Liquid
Triethanolamine
Carbopol 934
Acrylates/C10-30 Alkyl Crosspolymer
Aloe Barbadensis Leaf Juice
Hydrocloric Acid Reagent

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70392-020-04Stay Put Sunscreen SPF 30118 mL in 1 BOTTLELOTION1182

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70392-02070392-020-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
Stay Put Sunscreen SPF 30OCTINOXATE 7.50% OCTISALATE 5.00% OXYBENZONE 4.00% HOMOSALATE 10.00%Sawyer Products Inc7ecba495-a912-4697-8287-2e5836e610e12026-03-27WarningsExact identifier
ndc (package): 70392-020-04
ndc (product): 70392-020
ndc11 (package): 70392002004
spl id: 4e0242e2-28ba-8c42-e063-6294a90a7d01
spl set id: 7ecba495-a912-4697-8287-2e5836e610e1

Reported adverse events (FAERS/openFDA)#

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