85435-003 TALLOW SUNSCREEN

TALLOW SUNSCREEN by

Drug Labeling and Warnings

TALLOW SUNSCREEN by is a Otc medication manufactured, distributed, or labeled by Guangdong Renhe Guozhuang Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

TALLOW SUNSCREEN- tallow sunscreen cream 
Guangdong Renhe Guozhuang Biotechnology Co., Ltd.

----------

85435-003
TALLOW SUNSCREEN

Active Ingredient(s)

JOJOBA SEED OIL 3%

TOCOPHEROL 1%

TALLOW 8%

Purpose

Moisturizing
Antioxidant
Nourishing

Use

Helps protect skin from harmful sun exposure and prevent sunburn.

Warnings

Warnings For external use only.

Do not use

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

●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.

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

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

Directions

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

Other information

No

Inactive ingredients

Aqua, Non-nano Zinc Oxide, Beeswax

Package Label - Principal Display Panel

undefined

TALLOW SUNSCREEN 
tallow sunscreen cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 85435-003
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TOCOPHEROL (UNII: R0ZB2556P8) (TOCOPHEROL - UNII:R0ZB2556P8) TOCOPHEROL1 g  in 100 g
TALLOW (UNII: 98HPY76U4W) (TALLOW - UNII:98HPY76U4W) TALLOW8 g  in 100 g
JOJOBA OIL (UNII: 724GKU717M) (JOJOBA OIL - UNII:724GKU717M) JOJOBA OIL3 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
AQUA (UNII: 059QF0KO0R)  
ZINC OXIDE (UNII: SOI2LOH54Z)  
BEESWAX (UNII: 2ZA36H0S2V)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 85435-003-0160 g in 1 BOTTLE; Type 0: Not a Combination Product04/03/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02004/03/202512/31/2025
Labeler - Guangdong Renhe Guozhuang Biotechnology Co., Ltd. (619052164)
Establishment
NameAddressID/FEIBusiness Operations
Guangdong Renhe Guozhuang Biotechnology Co., Ltd.619052164manufacture(85435-003)

Revised: 1/2026
 
Guangdong

© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.