SURFACE X CUTIE PALS HAND SANITIZER CITRUS CRUSH- alcohol liquid

Surface x Cutie Pals Hand Sanitizer Citrus Crush by

Drug Labeling and Warnings

Surface x Cutie Pals Hand Sanitizer Citrus Crush by is a Otc medication manufactured, distributed, or labeled by Longway Technology(Guangzhou)Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

Ethyl Alcohol 70% v/v.

Purpose

Antibacterial

Uses

• For hand-washing to help reduce bacteria on the skin

Warnings

For external use only.

Flammable, keep away from fire and flames

When using this product

• test on a small area of skin before full use.
• keep out of eyes. In case of contact with eyes, flush thoroughly with water.
• Avoid contact with broken skin.
• Do not inhale or ingest.

Stop use and ask doctor if

• allergy, irritation or redness develops.
• Condition persists for more than 72 hours.

Keep out of reach of children.

• If product is swallowed, get medical help or contact a poison control center right away.

Directions

• Spray hands with product and allow to dry without wiping.
• For children under 6, use only under adult supervision.
• Not recommended for infants.

Other information

• Do not store above 105 °F May discolor some fabrics
• Harmful to wood finishes and plastics

Inactive ingredients

WATER (AQUA), FRAGRANCE (PARFUM), LIMONENE, MENTHA VIRIDIS (SPEARMINT) LEAF OIL.

Questions or comments?

1-212- 244-5170info@amora.beauty

Package Labeling:

INGREDIENTS AND APPEARANCE

SURFACE X CUTIE PALS HAND SANITIZER CITRUS CRUSH 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85161-012
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
SPEARMINT (UNII: J7I2T6IV1N)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85161-012-01	45 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/02/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	10/02/2025

Labeler - Longway Technology(Guangzhou)Co., Ltd. (844528915)

Registrant - Longway Technology(Guangzhou)Co., Ltd. (844528915)