Surfblok Lip Balm Box

Manufacturer: Arizona Sun Products
Effective date: 2026-04-09
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 01:53:18

Label at a glance#

ProductArizona Sun ProductsSurfblok Lip Balm SPF 15

Active ingredientOXYBENZONE, OCTINOXATE

Label structure9 sections

Indications and uses

Provides minimal sunburn protection. Higher SPF gives more sunburn protection

Dosage and administration

Use anytime and apply liberally to the lips 30 minutes before and during sun exposure. Reapply after swimming and exercise. Use on children under the age of six months only wih the advise of a physician.

Contacts and useful links#

PhoneLabel contact1-800-442-4786

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Octinoxate 7.50%, Oxybenzone 3.00%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

Provides minimal sunburn protection. Higher SPF gives more sunburn protection

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

Stop and ask a doctor

OTC - STOP USE SECTION

if rash or irritation develops and lasts.

Keep out of the reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed get medical help or contact a poison control center right away.

Directions

INSTRUCTIONS FOR USE SECTION

Other Information

OTHER SAFETY INFORMATION

Sun Alert: Limiting sun exposure, wearing protective clothing, and using suscreen may reduce the risk of skin aging, skin cancer and other harmful effects of the sun.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Extract, Cera Alba (Beeswax), Flavor, Helianthus Annuus (Sunflower) Seed Oil (and) Carthamus Tinctorius (Safflower) Oil (and) Styrene/Butadiene Copolymer, Paraffinum Liquidum (Mineral Oil), Propylparaben, Ricinus Communis (Castor) Seed Oil, Simmondsia Chinensis (Jojoba) Oil, Tocopheryl Acetate (Vitamin E).

Questions or Comments?

OTC - QUESTIONS SECTION

Call toll free 1-800-442-4786

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

surfblokdrugfacts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
61973-405-10	Arizona Sun ProductsSurfblok Lip Balm SPF 15	153 g in 1 CARTON	LIPSTICK	153		2

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

Arizona Sun ProductsSurfblok Lip Balm SPF 15
Lip Balm
OXYBENZONE
SUNFLOWER SEED
SAFFLOWER OIL
ALOE VERA LEAF
OCTINOXATE
WHITE WAX
CASTOR OIL
MINERAL OIL
SIMMONDSIA CHINENSIS SEED
.ALPHA.-TOCOPHEROL ACETATE
PROPYLPARABEN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
61973-405	61973-405-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
OXYBENZONE	95OOS7VE0Y	ACTIB
SUNFLOWER SEED	R9N3379M4Z	IACT
SAFFLOWER OIL	65UEH262IS	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
OCTINOXATE	4Y5P7MUD51	ACTIB
WHITE WAX	7G1J5DA97F	IACT
CASTOR OIL	D5340Y2I9G	IACT
MINERAL OIL	T5L8T28FGP	IACT
SIMMONDSIA CHINENSIS SEED	D24K2Q1F6H	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
PROPYLPARABEN	Z8IX2SC1OH	IACT

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Arizona Sun ProductsSurfblok Lip Balm SPF 15	LIP BALM	Arizona Sun Products	11fdbae5-84ec-7b1d-e063-6294a90a2878	2026-04-09	Warnings	Exact identifier ndc (product): 61973-405
Arizona Sun ProductsSurfblok Lip Balm SPF 15	LIP BALM	Arizona Sun Products	11fdcfd0-8b24-7efc-e063-6294a90af7fa	2026-04-09	Warnings	Exact identifier ndc (package): 61973-405-10 ndc (product): 61973-405 ndc11 (package): 61973040510 spl id: 4f0bf434-dd3f-cd91-e063-6394a90a3397 spl set id: 11fdcfd0-8b24-7efc-e063-6294a90af7fa

Reported adverse events (FAERS/openFDA)#

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