FDA.reportPublic FDA data

ULTRALIGHT AGE DEFENSE SPF 50

Manufacturer
Guangzhou Origin Beauty Cosmetics Co., Ltd.
Effective date
2026-03-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:52:15

Label at a glance#

ProductULTRALIGHT AGE DEFENSE SPF 50
Active ingredientZINC OXIDE
Label structure14 sections

Label contents#

Full prescribing information#

OTC - ASK DOCTOR/PHARMACIST SECTION

Children under 6 months please ask a doctor

Stop use and ask a doctor if rash occurs

Active ingredient section

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide SOI2LOH54Z

Do not use section

OTC - DO NOT USE SECTION

For external use only

Do not use on damaged or broken skin.

When using the product Keep out of eyes.

Rinse with water to remove.

Stop use and ask a doctor if rash occurs.

Keep out of reach of children.

If swallowed, get medical help or contact

Poison Control Center right away.

Directions Apply liberally 15 minutes before sun exposure

Reapply: After 40 minutes of swimming

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Pregnancy or breast feeding section

OTC - PREGNANCY OR BREAST FEEDING SECTION

Ask for doctor

Purpose section

OTC - PURPOSE SECTION


PROTECT + HYDRATE + RESTORE


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

Questions section

OTC - QUESTIONS SECTION

If you have any questions, please contact the following website

www.himalayacosmetic.com

OTC - STOP USE SECTION


Stop use and ask a doctor if rash occurs.

OTC - WHEN USING SECTION


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 sun protection measures
including: Limit time in the sun,especially from 10a.m. - 2p.m.

WARNINGS SECTION

For external use only
Do not use on damaged or broken skin.
When using the product Keep out of eyes.
Rinse with water to remove.
Stop use and ask a doctor if rash occurs.
Keep out of reach of children.
If swallowed, get medical help or contact
Poison Control Center right away.
Directions Apply liberally 15 minutes
before sun exposure
Reapply: After 40 minutes of swimming

INACTIVE INGREDIENT SECTION

Water
Glycerin
Butyrospermum Parkii (Shea Butter)
Helianthus Annuus (Sunflower) Seed Oil
Arachidyl Alcohol
Behenyl Alcohol
Arachidyl Glucoside
Butyloctyl Salicylate
Polyhydroxystearic Acid
Bisabolol
Sodium Hyaluronate
Tocopherol
Caprylhydroxamic Acid
Caprylyl Glycol
Sodium Stearoyl Glutamate
Sodium Gluconate
Citric Acid

INDICATIONS & USAGE SECTION

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

DOSAGE & ADMINISTRATION SECTION

At least every 2 hours

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

bottlebottleout packageout packageThe specification of this product is 50mL per bottle. The style of the bottle body and the outer material is shown in the picture

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87545-001-01ULTRALIGHT AGE DEFENSE SPF 5050 g in 1 BOTTLE, PLASTICLOTION501

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87545-00187545-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM STEAROYL GLUTAMATE65A9F4P024IACT
TOCOPHEROLR0ZB2556P8IACT
BUTYROSPERMUM PARKII (SHEA) OILO88E196QRFIACT
CAPRYLHYDROXAMIC ACIDUPY805K99WIACT
CAPRYLYL GLYCOL00YIU5438UIACT
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL3W1JG795YIIACT
SODIUM HYALURONATEYSE9PPT4THIACT
CITRIC ACID2968PHW8QPIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
BEHENYL ALCOHOL9G1OE216XYIACT
ARACHIDYL ALCOHOL1QR1QRA9BUIACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
ZINC OXIDESOI2LOH54ZACTIB
SODIUM GLUCONATER6Q3791S76IACT
AQUA059QF0KO0RIACT
ARACHIDYL GLUCOSIDE6JVW35JOOJIACT
BISABOLOL24WE03BX2TIACT
GLYCERINPDC6A3C0OXIACT

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
ULTRALIGHT AGE DEFENSE SPF 50ZINC OXIDEGuangzhou Origin Beauty Cosmetics Co., Ltd.4e36a743-7906-2b7b-e063-6294a90af3142026-03-29WarningsExact identifier
ndc (package): 87545-001-01
ndc (product): 87545-001
ndc11 (package): 87545000101
spl id: 4e36a743-7907-2b7b-e063-6294a90af314
spl set id: 4e36a743-7906-2b7b-e063-6294a90af314

Reported adverse events (FAERS/openFDA)#

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