Lip Balm SPF15 ( 2533)

Manufacturer: Cosmuses Cosmetics (Ningbo) Co., Ltd.
Effective date: 2026-08-07
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: daily-update
Hydrated at: 2026-08-11 01:01:12

Label at a glance#

Productlip balm SPF15( 2533) 01

Active ingredientHOMOSALATE, OCTOCRYLENE, AVOBENZONE, OCTISALATE

Label structure10 sections

Indications and uses

Helps prevent sunburn

Dosage and administration

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

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Octocrylene 3%

Homosalate 5%

Avobenzone 2%

Octisalate 3%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

Helps prevent sunburn

WARNINGS SECTION

For external use only.

Do not Use on Damaged or Broken Skin

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs.

OTC - WHEN USING SECTION

When using this product keep out of eyes. Rinse with water to remove.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

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

ROUTE, METHOD AND FREQUENCY OF ADMINISTRATION

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 value of 15 or higher and other sunprotection measures including:*Limit time in the sun, especially from10am to 2 pm.* Wear long sleeved shirts, pants, hats, and sunglasses

Inactive ingredients

INACTIVE INGREDIENT SECTION

Mineral oil, petrolatum, ozokerite, polyisobutene, ethylhexyl palmitate,beeswax, butyrospermum parkii (shea) butter, microcrystalline wax,phenoxyethanol, fragrance, BHT

OTC - QUESTIONS SECTION

questions?

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

principal display panel 82953-073-01

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

lip balm SPF15( 2533) 01
Avobenzone,Homosalate,Octocrylene,Octisalate
HOMOSALATE
OCTOCRYLENE
AVOBENZONE
OCTISALATE
PETROLATUM
ETHYLHEXYL PALMITATE
MINERAL OIL
CERESIN
FRAGRANCE 13576
MICROCRYSTALLINE WAX
POLYISOBUTYLENE (1000 MW)
BUTYROSPERMUM PARKII (SHEA) BUTTER
PHENOXYETHANOL
BEESWAX
BHT

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
82953-073	82953-073-01, 82953-073-02, 82953-073-03, 82953-073-04, 82953-073-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
HOMOSALATE	V06SV4M95S	ACTIB
OCTOCRYLENE	5A68WGF6WM	ACTIB
AVOBENZONE	G63QQF2NOX	ACTIB
OCTISALATE	4X49Y0596W	ACTIB
PETROLATUM	4T6H12BN9U	IACT
ETHYLHEXYL PALMITATE	2865993309	IACT
MINERAL OIL	T5L8T28FGP	IACT
CERESIN	Q1LS2UJO3A	IACT
FRAGRANCE 13576	5EM498GW35	IACT
MICROCRYSTALLINE WAX	XOF597Q3KY	IACT
POLYISOBUTYLENE (1000 MW)	5XB3A63Y52	IACT
BUTYROSPERMUM PARKII (SHEA) BUTTER	K49155WL9Y	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
BEESWAX	2ZA36H0S2V	IACT
BHT	1P9D0Z171K	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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
lip balm SPF15( 2533) 01	AVOBENZONE,HOMOSALATE,OCTOCRYLENE,OCTISALATE	Cosmuses Cosmetics (Ningbo) Co., Ltd.	5870aa44-1375-cdc5-e063-6394a90af4a5	2026-08-07	Warnings	Exact identifier ndc (package): 82953-073-04 ndc (package): 82953-073-05 ndc (package): 82953-073-03 ndc (package): 82953-073-02 ndc (package): 82953-073-01 ndc (product): 82953-073 ndc11 (package): 82953007303 ndc11 (package): 82953007302 ndc11 (package): 82953007305 ndc11 (package): 82953007301 ndc11 (package): 82953007304 spl id: 5870aa5e-0714-cdf4-e063-6394a90a6461 spl set id: 5870aa44-1375-cdc5-e063-6394a90af4a5

Reported adverse events (FAERS/openFDA)#

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