AMORA HAND SANITIZER MIST CHERRY- ethyl alcohol liquid

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

Alcohol 70% v/v

INACTIVE INGREDIENT

WATER (AQUA), FRAGRANCE (PARFUM), PRUNUS CERASUS(BITTER CHERRY) EXTRACT,BUTYLENE GLYCOL,HYDROXYACETOPHENONE.

KEEP OUT OF REACH OF CHILDREN

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

QUESTIONS

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

OTHER SAFETY INFORMATION

Do not store above 105 °F

May discolor some fabrics
Harmful to wood finishes and plastics

PURPOSE

Antibacterial

WARNINGS

Warnings
For external use only.
Flammable, keep away from fire and flames
When using this product
est 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

rritation 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.

DOSAGE & ADMINISTRATION

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

INDICATIONS & USAGE

For hand-washing to decrease bacteria on the skin.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AMORA HAND SANITIZER MIST CHERRY 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85161-171
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PRUNUS CERASUS (BITTER CHERRY) FRUIT EXTRACT (UNII: 1L29G6428X)
FRAGRANCE 13576 (UNII: 5EM498GW35)

Product Characteristics
Color		Score
Shape	FREEFORM	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85161-171-01	45 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/01/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	02/01/2026

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

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

Establishment
Name	Address	ID/FEI	Business Operations
Longway Technology(Guangzhou)Co.,Ltd.		844528915	manufacture(85161-171)