Zep Sun Screen Towels

Manufacturer: Zep Inc.
Effective date: 2018-11-14
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-02 00:47:09

Label at a glance#

ProductZep Sun Screen Towels

Active ingredientOXYBENZONE

Label structure10 sections

Indications and uses

-Provides high protection against sunburn -Retains SPF after 80 minutes of sweating activity or activity in the water.

Dosage and administration

• Unfold towel • Apply evenly before sun exposure • For children under 6 months, consult a doctor • Reapply after towel drying, swimming or sweating

Contacts and useful links#

PhoneLabel contact1-877-428-9937

Label contents#

Full prescribing information#

Uses

USE IN SPECIFIC POPULATIONS SECTION

-Provides high protection against sunburn
-Retains SPF after 80 minutes of sweating activity or activity in the water.

For external use only.

WARNINGS SECTION

Flammable. Keep away from heat and flame when applying this product.

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor

OTC - STOP USE SECTION

if rash or irritation develops and lasts

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

• Unfold towel
• Apply evenly before sun exposure
• For children under 6 months, consult a doctor
• Reapply after towel drying, swimming or sweating

INACTIVE INGREDIENT SECTION

Ethanol

Questions or comments?

OTC - QUESTIONS SECTION

Call 1-877-I-BUY-ZEP (1-877-428-9937)

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Oxybenzone (5%).....................................Sunscreen

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sunscreen Towels

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

Zep Sun Screen Towels
Oxybenzone
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
66949-421	66949-421-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	IACT
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
7aa66f25-accf-4ee6-e053-2991aa0a9a17			318e2416-31e8-3baa-e054-00144ff88e88	2018-11-14	Warnings	Exact identifier spl id: 7aa66f25-accf-4ee6-e053-2991aa0a9a17 spl set id: 318e2416-31e8-3baa-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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