Blumen Advance Hand Sanitizer Wipes Clear

Blumen Advance Hand Sanitizer Wipes Clear by

Drug Labeling and Warnings

Blumen Advance Hand Sanitizer Wipes Clear by is a Otc medication manufactured, distributed, or labeled by 4E BRANDS NORTHAMERICA, LLC, HangZhou YangYi Daily Cosmetics Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BLUMEN ADVANCE HAND SANITIZER WIPES CLEAR- benzalkonium chloride cloth 
4E BRANDS NORTHAMERICA, LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Blumen Advance Hand Sanitizer Wipes Clear

Drug Facts

Activeingredients

Benzalkonium Chloride 0.13%

Purpose

Antibacterial 

Uses

• Hand sanitizer to help reduce bacteria on the skin

Warnings

• 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 doctor if 

irritation or rash apperars and lasts.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

- Wet hands thoroughly with product and allow to dry

- Discard wipes in trash receptacle after use. Do not flush

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

Inactive ingredients

Water, Glycerin, Ethylhexylglycerin, Phenoxyethanol, Didecyldimonium Chloride, Propylene Glycol, Parfum (Fragrance), Aloe Barbadensis Leaf Extract (Aloe Vera), Tocopheryl Acetate (Vitamin E).

Package Labeling:

BLUMEN ADVANCE HAND SANITIZER WIPES CLEAR 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70074-025
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70074-025-00	15 in 1 PACKAGE	07/05/2020	07/07/2020
1		0.12454 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/05/2020	07/07/2020

Labeler - 4E BRANDS NORTHAMERICA, LLC (076595687)

Establishment
Name	Address	ID/FEI	Business Operations
HangZhou YangYi Daily Cosmetics Technology Co., Ltd.		554479892	manufacture(70074-025)

Revised: 12/2021

Document Id: d2cbf516-496a-2ca2-e053-2995a90a9992

34390-5

Set id: 8bb32f35-0d12-40af-b6a5-4a5638bc7932

Version: 5

Effective Time: 20211210