FDA.reportPublic FDA data

NYU Langone Health Lip Balm

Manufacturer
Guangzhou Yilong Cosmetics Co., Ltd
Effective date
2025-06-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:03:52

Label at a glance#

ProductNYU Langone Health Lip Balm
Active ingredientZINC OXIDE
Label structure11 sections

Indications and uses

Helps prevent sunburn. If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 0.2%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

Helps prevent sunburn.
If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Warnings

WARNINGS SECTION

For external use only.

OTC - STOP USE SECTION

Stop use and ask 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 wate to remove.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. lf swallowed, getmedical help or contact
Poison Control Center right away.

Dosage

DOSAGE & ADMINISTRATION SECTION

Squeeze out an appropriate amount of Sunscreen lip balm and spread evenly on your lips.

Inactive ingredients

INACTIVE INGREDIENT SECTION

PETROLATUM：69%
CERA MICROCRISTALLINA：13%
BEESWAX：5%
SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL：5%
MINERAL OIL：4.4%
BUTYROSPERMUM PARKII(SHEA) BUTTER：2%
MEL：1%
COCOS NUCIFERA (COCONUT) OIL：0.2%
ROSMARINUS OFFICINALIS (ROSEMARY) LEAF OIL：0.2%

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74458-045-01NYU Langone Health Lip Balm5 g in 1 TUBELIPSTICK52

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
74458-04574458-045-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
MINERAL OILT5L8T28FGPIACT
ZINC OXIDESOI2LOH54ZACTIB
JOJOBA OIL724GKU717MIACT
SHEA BUTTERK49155WL9YIACT
YELLOW WAX2ZA36H0S2VIACT

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
38607ebb-28b0-15da-e063-6394a90aadc62444c361-cd40-2b48-e063-6394a90a7dcc2025-06-25WarningsExact identifier
spl id: 38607ebb-28b0-15da-e063-6394a90aadc6
spl set id: 2444c361-cd40-2b48-e063-6394a90a7dcc

Reported adverse events (FAERS/openFDA)#

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