SPF30 Sunscreen Stick

Manufacturer: Zhejiang Ayan Biotech Co.,Ltd.
Effective date: 2026-06-25
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: monthly-update
Hydrated at: 2026-07-17 21:35:50

Label at a glance#

ProductSPF30 Sunscreen

Active ingredientAVOBENZONE, HOMOSALATE, OCTOCRYLENE, OCTISALATE

Label structure10 sections

Indications and uses

Helps prevent sunburn.

Dosage and administration

Apply liberally 15 minutes before sun exposure. Usa a water resistant sunscreen if swimming or sweating. Reapply at least every 2 hours. Children under 6 months: Ask a doctor.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3% Octocrylene 10% Octisalate 5% Homosalate 10%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

Helps prevent sunburn.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

on damaged or broken skin.

When using 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 reash occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If product is swallowed, get medical help or contact a Poison Control right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply liberally 15 minutes before sun exposure.
Usa a water resistant sunscreen if swimming or sweating.
Reapply at least every 2 hours.
Children under 6 months: Ask a doctor.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Mineral Oil, Ozokerite, Cera Microcristallina, Polyisobutene, Cocos Nucifera (Coconut) Oil, Ethylhexyl Palmitate, Polyethylene, Tridencyl Trimellitate, Butyrospermum Parkii (Shea Butter), BHT, Tocopheryl Acetate, Fragrance.

Other Information

SPL UNCLASSIFIED SECTION

Protect from excessive heat and direct sun.

Questions?

OTC - QUESTIONS SECTION

Call AP Specialties

BATCH NO:

Distributed by:

SPF30 Sunscreen Stick, 18g (70412-211-18)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

SPF30 Sunscreen Stick, 15g (70412-211-15)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label4

Products#

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

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

SPF30 Sunscreen
AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OCTISALATE
MINERAL OIL
CERESIN
COCONUT OIL
ETHYLHEXYL PALMITATE
HIGH DENSITY POLYETHYLENE
TRIDECYL TRIMELLITATE
SHEA BUTTER
BUTYLATED HYDROXYTOLUENE
.ALPHA.-TOCOPHEROL ACETATE
AVOBENZONE
HOMOSALATE
OCTOCRYLENE
OCTISALATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70412-211	70412-211-18, 70412-211-15, 70412-211-12

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
MINERAL OIL	T5L8T28FGP	IACT
CERESIN	Q1LS2UJO3A	IACT
COCONUT OIL	Q9L0O73W7L	IACT
ETHYLHEXYL PALMITATE	2865993309	IACT
HIGH DENSITY POLYETHYLENE	UG00KM4WR7	IACT
TRIDECYL TRIMELLITATE	FY36J270ES	IACT
SHEA BUTTER	K49155WL9Y	IACT
BUTYLATED HYDROXYTOLUENE	1P9D0Z171K	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
AVOBENZONE	G63QQF2NOX	ACTIB
HOMOSALATE	V06SV4M95S	ACTIB
OCTOCRYLENE	5A68WGF6WM	ACTIB
OCTISALATE	4X49Y0596W	ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
3	2023-11-06	full-release	2026-05-31 23:59:18

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
SPF30 Sunscreen	AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OCTISALATE	Zhejiang Ayan Biotech Co.,Ltd.	6759b9f7-296a-4c06-9198-b4e824e0bdc9	2026-06-25	Warnings	Exact identifier ndc (package): 70412-211-12 ndc (package): 70412-211-15 ndc (package): 70412-211-18 ndc (product): 70412-211 ndc11 (package): 70412021118 ndc11 (package): 70412021112 ndc11 (package): 70412021115 spl id: 55169cbf-fece-892f-e063-6394a90ad351 spl set id: 6759b9f7-296a-4c06-9198-b4e824e0bdc9

Reported adverse events (FAERS/openFDA)#

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