79740-004 下架 Accel Hand Sanitizer

Accel Hand Sanitizer by

Drug Labeling and Warnings

Accel Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by ANTHOS GROUP, INC, THE. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACCEL HAND SANITIZER- hand sanitizer liquid 
ANTHOS GROUP, INC, THE

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79740-004 下架
Accel Hand Sanitizer

Active Ingredient(s)

Ethyl alcohol 75% v/v

Purpose

Antiseptic

Use

Hand sanitizer to help reduce bacteria on skin when soap & water not available

Warnings

Flammable.keep away from fire or flame.for external use only.when using this product do not use in or near the eyes.in case of contact rinse eyes thoroughly with water

Stop use and ask a doctoir ii irritation or rash appears andi lasts.

Keep out of reach Orf children. If swallowed get medical help or contact a Poison Control Center immediatelly.

Do not use

do not use in or near the eyes.in case of contact rinse eyes thoroughly with water

Stop use and ask a doctoir ii irritation or rash appears andi lasts.

when using this product do not use in or near the eyes.in case of contact rinse eyes thoroughly with water

Stop use and ask a doctoir ii irritation or rash appears andi lasts.

Keep out of reach Orf children. If swallowed get medical help or contact a Poison Control Center immediatelly.

Keep out of reach Orf children. If swallowed get medical help or contact a Poison Control Center immediatelly.

Directions

Put enough product in your palm to cover hands when rubibing together rubbriskly until dry children under 6 years of age should be supervised when using

Other information

store below 110°F (43°C)
May discollor certairn fabrics or surfaces

Inactive ingredients

Water(aqua), Carbomer, Cucumber Extract, Lemon Extract, Aminomethyl Proparnol, Aloe Leaf Extract, Glycerin

Package Label - Principal Display Panel

ACCEL HAND SANITIZER 
hand sanitizer liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79740-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CUCUMBER (UNII: YY7C30VXJT)
LEMON (UNII: 24RS0A988O)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79740-004-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
2	NDC: 79740-004-02	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	03/30/2020	02/28/2024

Labeler - ANTHOS GROUP, INC, THE (117511051)

Establishment
Name	Address	ID/FEI	Business Operations
ANTHOS GROUP, INC, THE		117511051	manufacture(79740-004)

Revised: 2/2024

Document Id: 126dff0c-5ca4-d8d2-e063-6294a90ae76b

34390-5

Set id: b1ada702-f90c-2b2a-e053-2995a90acbc1

Version: 3

Effective Time: 20240228