PURDOUX- sanitizing wet wipes cloth

Purdoux by

Drug Labeling and Warnings

Purdoux by is a Otc medication manufactured, distributed, or labeled by Choice One Medical Inc, ZHEJIANG RUOLIN HYGIENIC PRODUCTS CO., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Benzalkonium chloride 0.13%

Purpose

Antiseptic

Use

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

on children less than two months of age
near eyes or on on open skin wounds

WHEN USING

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 at 800-222-1222

STOP USE

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

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

Directions

Flip open dispensing cap. Locate wipe at center of roll via small opening of the lid. Close the lid cap after use.
Apply to hands and skin. No rinsing required. Discard after use.

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

Other information

Avoid freezing and store below 110F (43C).

Dispose the used wipe in trash, do not flush it into the toilet.

Inactive ingredients

aloe babadensis leaf juice, ethylhexylglycerin, fragrance, glycerin, propylene glycol, purified water USP

Package Label - Principal Display Panel

80 PCS NDC: 81796-123-13

INGREDIENTS AND APPEARANCE

PURDOUX 
sanitizing wet wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81796-123
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
FRAGRANCE CUCUMBER ALOE ORC1802955 (UNII: FSS3TH6V9M)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81796-123-11	10 in 1 CANISTER	04/20/2021
1		10 mL in 1 NOT APPLICABLE; Type 0: Not a Combination Product
2	NDC: 81796-123-12	35 in 1 CANISTER	04/20/2021
2		35 mL in 1 NOT APPLICABLE; Type 0: Not a Combination Product
3	NDC: 81796-123-13	80 in 1 CANISTER	04/20/2021
3		80 mL in 1 NOT APPLICABLE; Type 0: Not a Combination Product
4	NDC: 81796-123-14	130 in 1 CANISTER	04/20/2021
4		130 mL in 1 NOT APPLICABLE; Type 0: Not a Combination Product
5	NDC: 81796-123-15	400 in 1 CANISTER	04/20/2021
5		400 mL in 1 NOT APPLICABLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/20/2021

Labeler - Choice One Medical Inc (203387337)

Establishment
Name	Address	ID/FEI	Business Operations
ZHEJIANG RUOLIN HYGIENIC PRODUCTS CO., LTD		415426870	manufacture(81796-123)