DR JEFF HAND SANITIZER- ethyl alcohol gel

DR JEFF Hand Sanitizer by

Drug Labeling and Warnings

DR JEFF Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Jiefu (Ningbo, Zhejiang)Daily Chemicals Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug facts

Active Ingredient(s)

Ethyl Alcohol 75%±5

Purpose

Antimicrobial

Use

Helps reduce bacteria on the skin.

Warnings

Flammable.Keep away from fire or flame.

For external use only.

WHEN USING

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

STOP USE

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

KEEP OUT OF REACH OF CHILDREN

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

Directions

Place enough product in your palm to thoroughly spread on both hands and nub into the skin until dry.

Children under 6 years of age should be supervised when using this product.

Other information

Store below 106°F(41C)

May discolor certain fabrics or surfaces.

Inactive ingredients

Distilled water、Carbomer、glycerol、Aloe extract、triethanolamine

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

DR JEFF HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77266-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	750 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE (UNII: V5VD430YW9)	10 mg  in 1 mL
TROLAMINE (UNII: 9O3K93S3TK)	2 mg  in 1 mL
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)	3 mg  in 1 mL
GLYCERIN (UNII: PDC6A3C0OX)	20 mg  in 1 mL
WATER (UNII: 059QF0KO0R)	215 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77266-001-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/04/2020
2	NDC: 77266-001-02	104 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/04/2020
3	NDC: 77266-001-03	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/04/2020
4	NDC: 77266-001-04	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/04/2020
5	NDC: 77266-001-05	1020 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/04/2020
6	NDC: 77266-001-06	3780 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/04/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/04/2020

Labeler - Jiefu (Ningbo, Zhejiang)Daily Chemicals Co., Ltd (554532398)

Registrant - Jiefu (Ningbo, Zhejiang)Daily Chemicals Co., Ltd (554532398)

Establishment
Name	Address	ID/FEI	Business Operations
Jiefu (Ningbo, Zhejiang)Daily Chemicals Co., Ltd		554532398	manufacture(77266-001)