FDA.reportPublic FDA data

FEIBTH TALLOW SUNSCREEN

Manufacturer
Guangzhou Qiexiran Cosmetics Co., Ltd.
Effective date
2025-06-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:03:29

Label at a glance#

ProductFEIBTH TALLOW SUNSCREEN
Active ingredientZINC OXIDE
Label structure13 sections

Dosage and administration

·Apply liberally 15 minutes before sun exposure ·Reapply: 1.After 80 minutes of swimming or sweating 2.Immediately after towel drying 3.At least every 2 hours

Storage and handling

· Protect this product from excessive heat and direct sun · May stain some fabrics

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 15% (w/w)

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

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.

Do not use

OTC - DO NOT USE SECTION

· on damaged or broken skin

When Using

OTC - WHEN USING SECTION

· keep out of eyes. Rinse with water to remove.

Stop Use

OTC - STOP USE SECTION

· rash occurs

Ask Doctor

OTC - ASK DOCTOR SECTION

· rash occurs

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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:
1.After 80 minutes of swimming or sweating
2.Immediately after towel drying
3.At least every 2 hours

Other information

STORAGE AND HANDLING SECTION

· Protect this product from excessive heat and direct sun
· May stain some fabrics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Tallow, Beeswax, Red Raspberry Seed Oil, Carrot Seed Oil, Coconut Oil, Jojoba Oil, Shea Butter

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85817-002-01FEIBTH TALLOW SUNSCREEN60 g in 1 TUBECREAM601

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85817-00285817-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
RASPBERRY4N14V5R27WIACT
COCONUT OILQ9L0O73W7LIACT
TALLOW98HPY76U4WIACT
JOJOBA OIL724GKU717MIACT
ZINC OXIDESOI2LOH54ZACTIB
BEESWAX2ZA36H0S2VIACT
SHEA BUTTERK49155WL9YIACT
CARROT SEED OIL595AO13F11IACT

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
FEIBTH TALLOW SUNSCREENTALLOW SUNSCREENGuangzhou Qiexiran Cosmetics Co., Ltd.37ead2b1-12d4-af92-e063-6394a90af0d62025-06-19WarningsExact identifier
ndc (package): 85817-002-01
ndc (product): 85817-002
ndc11 (package): 85817000201
spl id: 37ead2b1-12d5-af92-e063-6394a90af0d6
spl set id: 37ead2b1-12d4-af92-e063-6394a90af0d6

Reported adverse events (FAERS/openFDA)#

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