79740-001 下架 TIDL Advanced Hand Sanitizer

TIDL Advanced Hand Sanitizer by

Drug Labeling and Warnings

TIDL Advanced 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]

TIDL ADVANCED HAND SANITIZER- alcohol sanitizer gel 
ANTHOS GROUP, INC, THE

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79740-001 下架 TIDL Advanced Hand Sanitizer

Active Ingredient(s)

ALCOHOL 75%

Purpose

ANTIMICROBIAL

Use

Hand sanitizer to help reduce bacteria on skin.

Warnings

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

Do not use

do not use in or near the eyes. In case

of contact, rinse eyes thoroughly with water.

Stop use and ask doctor if irritation or rash appears and lasts

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

Keep out of reach of children If swallowed, get medical help or contact a poison Control center right away

Directions

Put enough product in your palm to cover hands and rub hands together briskly until dry
Children under 6 years of age should be supervised when using this product.

Other information

Store below11oF(43℃)
May discolor certain fabrics or surfaces

Inactive ingredients

Water(Aqua), Glycerin, Triethaolamine,Carbomer

Package Label - Principal Display Panel

TIDL ADVANCED HAND SANITIZER 
alcohol sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79740-001
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
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79740-001-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
2	NDC: 79740-001-02	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
3	NDC: 79740-001-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
4	NDC: 79740-001-04	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
5	NDC: 79740-001-05	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
6	NDC: 79740-001-06	180 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
7	NDC: 79740-001-07	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
8	NDC: 79740-001-08	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
9	NDC: 79740-001-09	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
10	NDC: 79740-001-10	1000 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(79740-001)

Revised: 2/2024

Document Id: 126dff0c-5ca3-d8d2-e063-6294a90ae76b

34390-5

Set id: ab063bb1-09f2-7e35-e053-2a95a90ab26e

Version: 4

Effective Time: 20240228