VEAKSON BEEF TALLOW SUNSCREEN- zinc oxide,phenylbenzimidazole sulfonic acid cream

VEAKSON BEEF TALLOW SUNSCREEN by

Drug Labeling and Warnings

VEAKSON BEEF TALLOW SUNSCREEN by is a Otc medication manufactured, distributed, or labeled by Guangdong Aimu Biological Technology Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

ZINC OXIDE 20%
PHENYLBENZIMIDAZOLE SULFONIC ACID 1%

Purpose

Sunscreen

Uses

Ensure skin is clean and dry before use.

Shake well before use.
Apply generously 15 minutes before sun exposure;
Reapply: every 2 hours or immediately after swimming, sweating, or towel drying.

Minimize sun exposure, especially between 10 AM and 2 PM, and wear long-sleeved clothing, long pants, a hat, and sunglasses;
For children under 6 months: Consult a doctor.

Warnings

For external use only.

SkinCancer/SkinAging Alert :Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, notskin cancer or early skin aging.

Stop Use

If a rash develops or the product is swallowed, seek medical assistance immediately

Do Not Use

Do not use on damaged or broken skin.

When Using

Avoid contact with eyes. If contact occurs, rinse immediately with water.

Keep Out Of Reach Of Children

Keep out of reach of children.

If a rash develops or the product is swallowed, seek medical assistance immediately.

Inactive ingredients

WATER 31.76%
ETHYLHEXYL SALICYLATE 5%
ADEPS BOVIS 5%
C12-15 ALKYL BENZOATE 4%
CETEARYL ALCOHOL 3.5%
SQUALANE 3%
DIMETHICONE 3%
GLYCERYL STEARATE 3%
ISONONYL ISONONANOATE 3%
BUTYROSPERMUM PARKII (SHEA) BUTTER 3%
SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL 3%
OLEA EUROPAEA (OLIVE) FRUIT OIL 2%
BEESWAX 2%
SILICA 2%
TOCOPHERYL ACETATE 1%
C20-24 ALKYL DIMETHICONE 1%
XANTHAN GUM 0.6%
CETETH-2 0.5%
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE 0.5%
SAURURUS CHINENSIS LEAF/ROOT EXTRACT 0.5%
TARAXACUM OFFICINALE (DANDELION) LEAF EXTRACT 0.5%
STEPHANIA TETRANDRA EXTRACT 0.5%
PHENOXYETHANOL 0.45%
LECITHIN 0.1%
ETHYLHEXYLGLYCERIN 0.05%
DISODIUM EDTA 0.02%
CI 77492 0.02%

Dosage & administration

Apply generously 15 minutes before sun exposure.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

VEAKSON BEEF TALLOW SUNSCREEN 
zinc oxide,phenylbenzimidazole sulfonic acid cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83566-563
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	20 g  in 100 g
PHENYLBENZIMIDAZOLE SULFONIC ACID (UNII: 9YQ9DI1W42) (PHENYLBENZIMIDAZOLE SULFONIC ACID - UNII:9YQ9DI1W42)	PHENYLBENZIMIDAZOLE SULFONIC ACID	1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
STEPHANIA TETRANDRA WHOLE (UNII: 7S7TV2F4XC)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CI 77492 (UNII: EX438O2MRT)
CETETH-2 (UNII: 7H8VAM7778)
SAURURUS CHINENSIS WHOLE (UNII: 6DRV3D37XS)
C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
SILICA (UNII: ETJ7Z6XBU4)
SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL (UNII: 724GKU717M)
DIMETHICONE (UNII: 92RU3N3Y1O)
SOYBEAN LECITHIN (UNII: 1DI56QDM62)
ETHYLHEXYL SALICYLATE (UNII: 4X49Y0596W)
OLEA EUROPAEA (OLIVE) FRUIT OIL (UNII: 6UYK2W1W1E)
BEESWAX (UNII: 2ZA36H0S2V)
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
SQUALANE (UNII: GW89575KF9)
BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
EDETATE DISODIUM (UNII: 7FLD91C86K)
XANTHAN GUM (UNII: TTV12P4NEE)
WATER (UNII: 059QF0KO0R)
TARAXACUM OFFICINALE (DANDELION) ROOT (UNII: 9DE5YCO0RU)
ADEPS BOVIS (UNII: 98HPY76U4W)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83566-563-01	60 g in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	01/04/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/04/2026

Labeler - Guangdong Aimu Biological Technology Co., Ltd (712647107)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Aimu Biological Technology Co., Ltd		712647107	manufacture(83566-563)