TALLOW SUNSCREEN

Manufacturer
Guangdong Renhe Guozhuang Biotechnology Co., Ltd.
Effective date
2025-04-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:39:57

Label at a glance#

ProductTALLOW SUNSCREEN
Active ingredientTOCOPHEROL, TALLOW, JOJOBA OIL
Label structure12 sections

Dosage and administration

●Apply to dlean, dry skin at least 15 minutes before sun exposure. ●Reapply every 2 hours, especially after swimming or sweating.

Storage and handling

No

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

JOJOBA SEED OIL 3%

TOCOPHEROL 1%

TALLOW 8%

Purpose

OTC - PURPOSE SECTION

Moisturizing
Antioxidant
Nourishing

Use

INDICATIONS & USAGE SECTION

Helps protect skin from harmful sun exposure and prevent sunburn.

Warnings

WARNINGS SECTION

Warnings For external use only.

Do not use

OTC - DO NOT USE SECTION

●if you have damaged or broken skin.
●If you have a history of skin allergies or sensitivities.

OTC - WHEN USING SECTION

●Avoid contact with eyes. If contact occurs, rinse thoroughly with water.
●Stop use and ask a doctor if rash or iritation develops and lasts.
●If swallowed, get medical help or contact Poison Control immediately.

OTC - STOP USE SECTION

●Stop use and ask a doctor if rash or iritation develops and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

This product is not child-resistant. Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

●Apply to dlean, dry skin at least 15 minutes before sun exposure.
●Reapply every 2 hours, especially after swimming or sweating.

Other information

STORAGE AND HANDLING SECTION

No

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, Non-nano Zinc Oxide, Beeswax

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
85435-003TALLOW SUNSCREEN CREAM [GUANGDONG RENHE GUOZHUANG BIOTECHNOLOGY CO., LTD.]1Unmatched20250406_31dc720d-7d7b-8dea-e063-6394a90aaa58.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85435-00385435-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
4855f8a8-f1ed-8a5f-e063-6394a90a4bbf31dc720d-7d7b-8dea-e063-6394a90aaa582026-01-14WarningsExact identifier
spl set id: 31dc720d-7d7b-8dea-e063-6394a90aaa58

Reported adverse events (FAERS/openFDA)#

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