SPF 30 Stay Put Sunscreen Lotion

Manufacturer: Sawyer Products
Effective date: 2016-01-15
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 22:44:37

Label at a glance#

ProductSPF 30 Stay Put Sunscreen

Active ingredientHOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE

Label structure7 sections

Indications and uses

Helps prevent sunburn.

Dosage and administration

Apply liberally to cool, dry skin 15 minutes before sun exposure. Use a water resistant sunscreen if swimming or sweating. Reapply at least every 2 hours. For children under 6 months of age: ask a doctor before using.

Label contents#

Full prescribing information#

Active ingredients:

OTC - ACTIVE INGREDIENT SECTION

Homosalate 10.0%, Octinoxate 7.5%, Octisalate 5.0%, Oxybenzone 4.0%

Purpose:

OTC - PURPOSE SECTION

Sunscreen

Uses:

INDICATIONS & USAGE SECTION

Helps prevent sunburn.

Warnings:

WARNINGS SECTION

Skin Cancer/Skin Aging Alert
Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to prevent sunburn, not
skin cancer or early skin aging.

For external use only.

Do not use

OTC - DO NOT USE SECTION

on broken or damaged skin.

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.

When using this product

OTC - WHEN USING SECTION

keep out of eyes. Rinse with warm water to remove.

Stop use and ask

OTC - STOP USE SECTION

a doctor if rash occurs.

Directions:

DOSAGE & ADMINISTRATION SECTION

Apply liberally to cool, dry skin 15 minutes before sun exposure.
Use a water resistant sunscreen if swimming or sweating.
Reapply at least every 2 hours.
For children under 6 months of age: ask a doctor before using.

Other information:

SPL UNCLASSIFIED SECTION

Protect this product container from excessive heat and direct sun.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Juice, Carbomer, Cetyl Alcohol, DEA-Cetyl Phosphate, DMDM
Hydantoin (and) Iodopropynyl Butylcarbamate, Hydrogenated Polyisobutene, Stearic Acid, Triethanolamine, Water.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer package1Inner package1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70392-012-01	2020-01-31	C162847	48780-1	9d75b9cf-fc29-f424-e053-dadaa90a57ce	SPF 30 Stay Put Sunscreen Lotion

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70392-012-01	SPF 30 Stay Put Sunscreen	1 in 1 CARTON	LOTION	1		2
70392-012-01	SPF 30 Stay Put Sunscreen	237 mL in 1 TUBE	LOTION	237		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70392-012	SPF 30 STAY PUT SUNSCREEN (HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE) LOTION [SAWYER PRODUCTS]	2	Legacy NDC, 2 package rows	20160116_1291e0a8-fb1a-4e76-8980-c72049bb5b9d.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

SPF 30 Stay Put Sunscreen
HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE
ALOE VERA LEAF
CARBOXYPOLYMETHYLENE
CETYL ALCOHOL
DIETHANOLAMINE CETYL PHOSPHATE
DMDM HYDANTOIN
IODOPROPYNYL BUTYLCARBAMATE
STEARIC ACID
TROLAMINE
WATER
HOMOSALATE
OCTINOXATE
OCTISALATE
OXYBENZONE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70392-012	70392-012-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALOE VERA LEAF	ZY81Z83H0X	IACT
CARBOXYPOLYMETHYLENE	0A5MM307FC	IACT
CETYL ALCOHOL	936JST6JCN	IACT
DIETHANOLAMINE CETYL PHOSPHATE	4UG0316V9S	IACT
DMDM HYDANTOIN	BYR0546TOW	IACT
IODOPROPYNYL BUTYLCARBAMATE	603P14DHEB	IACT
STEARIC ACID	4ELV7Z65AP	IACT
TROLAMINE	9O3K93S3TK	IACT
WATER	059QF0KO0R	IACT
HOMOSALATE	V06SV4M95S	ACTIB
OCTINOXATE	4Y5P7MUD51	ACTIB
OCTISALATE	4X49Y0596W	ACTIB
OXYBENZONE	95OOS7VE0Y	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
2963dbcd-09f1-6c51-e054-00144ff8d46c			1291e0a8-fb1a-4e76-8980-c72049bb5b9d	2016-01-15	Warnings	Exact identifier spl id: 2963dbcd-09f1-6c51-e054-00144ff8d46c spl set id: 1291e0a8-fb1a-4e76-8980-c72049bb5b9d

Reported adverse events (FAERS/openFDA)#

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