GZE LIP BALM

Manufacturer
Guangzhou Yilong Cosmetics Co., Ltd
Effective date
2024-10-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:31:16

Label at a glance#

ProductGZE LIP BALM
Active ingredientTOCOPHEROL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Tocopherol.

INACTIVE INGREDIENT SECTION

Helianthus Annuus (Sunflower) Seed Oil, Cera Alba, Simmondsia Chinensis (Jojoba) Seed Oil, Butyrospermum Parkii (Shea) Butter.

INDICATIONS & USAGE SECTION

Apply generously and evenly to lips 30 minutes before going out in the sun, or whenever they feel dry or chapped.

OTC - PURPOSE SECTION

Lip care

WARNINGS SECTION

For external use only.

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs.

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin.

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.

DOSAGE & ADMINISTRATION SECTION

Apply generously and evenly to lips 30 minutes before going out in the sun, or whenever they feel dry or chapped.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

product imageproduct image

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74458-282-012026-01-29C16284748780-149896155-a572-586f-e063-e6dba90add90GZE LIP BALM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74458-282-01GZE LIP BALM7 g in 1 TUBEPASTE71

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74458-282GZE LIP BALM (TOCOPHEROL 5%) PASTE [GUANGZHOU YILONG COSMETICS CO., LTD]11 package rows20241030_259b356e-2a02-320d-e063-6294a90af929.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74458-28274458-282-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
259b356e-2a03-320d-e063-6294a90af929259b356e-2a02-320d-e063-6294a90af9292024-10-29WarningsExact identifier
spl id: 259b356e-2a03-320d-e063-6294a90af929
spl set id: 259b356e-2a02-320d-e063-6294a90af929

Reported adverse events (FAERS/openFDA)#

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