FRESH FEELS HAND SANITIZER MIST VANILLA BREEZE SCENT- ethyl alcohol spray

FRESH FEELS HAND SANITIZER MIST VANILLA BREEZE SCENT by

Drug Labeling and Warnings

FRESH FEELS HAND SANITIZER MIST VANILLA BREEZE SCENT by is a Otc medication manufactured, distributed, or labeled by Amber Glow Cosmetics Limited. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

ETHYL ALCOHOL 70%

Purpose

ANTISEPTIC

Uses

To decrease bacteria on the skin that could cause disease.
When water, soap and towel are not available.
Recommended for repeated use.

Warnings

For external use only. Flammable. Keep away from fire or flame.

When using this product:
Keep out of eyes, ears, or mouth. In case of eye contact, flush eyes thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.

Stop use and ask a doctor if
Redness or irritation develop. Condition persists for more than 72 hours.

Keep out of reach of children.
Children should be supervised by an adult when using this product.
If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Spray product in your palm and rub hands together until dry.
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, Glycerin, Dipropylene Glycol, Glycereth-26, Fragrance, Butylene Glycol, Leuconostoc/Radish Root Ferment Filtrate, Aloe Barbadensis Leaf Juice, Phenoxyethanol. May Contain: Red 40 Lake (CI 16035), Red 33 Lake (CI 17200), Red 4 Lake (CI 14700), Yellow 5 Lake (CI 19140:1), Blue 1 Lake (CI 42090:2).

SPL UNCLASSIFIED SECTION

Distributed by: Amber Glow Cosmetics Limited
Unit 1806, 18/F., 9 Wing Hong Street,
Cheung Sha Wan, Hong Kong, Made in China
Questions or Comments call (877) 711-8333

Packaging

INGREDIENTS AND APPEARANCE

FRESH FEELS HAND SANITIZER MIST VANILLA BREEZE SCENT 
ethyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87302-208
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)
GLYCERIN (UNII: PDC6A3C0OX)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
GLYCERETH-26 (UNII: NNE56F2N14)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
FD&C RED NO. 40 ALUMINUM LAKE (UNII: 6T47AS764T)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
FD&C YELLOW NO. 5 ALUMINUM LAKE (UNII: JQ6BLH9FR7)
FD&C BLUE NO. 1 ALUMINUM LAKE (UNII: J9EQA3S2JM)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87302-208-08	35 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/07/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/07/2026

Labeler - Amber Glow Cosmetics Limited (765280476)