Revel Instant Hand Sanitizer (gel): (500 mL) NDC: 77716-015-16 (65 mL) NDC: 77716-01-02 (250 mL) NDC: 77716-015-25

Revel Instant Hand Sanitizer by

Drug Labeling and Warnings

Revel Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Sterling Perfumes Industries LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

REVEL INSTANT HAND SANITIZER- isopropyl alcohol gel 
Sterling Perfumes Industries LLC

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Revel Instant Hand Sanitizer (gel):
(500 mL) NDC: 77716-015-16
(65 mL) NDC: 77716-01-02
(250 mL) NDC: 77716-015-25

Active Ingredient(s)

Alcohol 75% v/v.

Purpose

Antiseptic

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

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

Do not use

• in children less than 2 months of age
• on open skin wounds

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

Aloe Barbadensis Leaf Extract, Aminomethyl Propanol, Carbomer, Fragrance, Glycerin, Isopropyl Myristate, Propylene Glycol, Tocopheryl Acetate, Water.

Package Label - Principal Display Panel

Manufactured by Sterling Perfumes Industries, LLC

Revel Instant Hand Sanitizer (500 mL) NDC: 77716-015-16

Revel Instant Hand Sanitizer (65 mL) NDC: 77716-015-02

Revel Instant Hand Sanitizer (250 mL) NDC: 77716-015-25

REVEL INSTANT HAND SANITIZER 
isopropyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77716-015
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
ALOE (UNII: V5VD430YW9)
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77716-015-16	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/26/2020
2	NDC: 77716-015-02	65 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/26/2020
3	NDC: 77716-015-08	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/29/2020	06/29/2020
4	NDC: 77716-015-25	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/29/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	06/26/2020	12/30/2024

Labeler - Sterling Perfumes Industries LLC (561432456)

Revised: 1/2025

Document Id: 2c4137db-d65e-945e-e063-6294a90a796d

34390-5

Set id: a901ab33-36c0-c136-e053-2a95a90afda2

Version: 4

Effective Time: 20250121