SWET PROTECT- benzalkonium chloride solution

SWET Protect by

Drug Labeling and Warnings

SWET Protect by is a Otc medication manufactured, distributed, or labeled by Energía 5 Mas 1 Comercio, S.A. de C.V., L Squared Global. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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*Effective at eliminating 99.9% of most common germs that may cause illness.

Drug Facts

Active Ingredient & Purpose

• Active ingredient: Purpose
• Benzalkonium Chloride 0.13% v/v..........................................................................................................................................: Antiseptic

Uses

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only.

Do not use

• on children less than 2 months of age
• on open skin wounds

When using this product

When using this product keep out of eyes. 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.

Directions

• place enough product on hands to cover all surfaces. Rub hands together until dry.
• supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• store between 68-77˚F (20-25˚C)
• do not expose to excessive heat

TAMPER EVIDENT: Do not use if the sealable tab is open or torn.

Inactive ingredients

allantoin, benzyl alcohol, edetate sodium, fragrance, glycerin, phenoxyethanol, polyoxyl 40 hydrogenated castor oil, propylene glycol, sodium hydroxide, trisodium nitrilotriacetate, water

Questions or comments?

+1-844-512 4626 (M-F) 9AM to 5 PM CDT or www.s-wet.com.mx

Package Label - Principal Display Panel

Kills 99.9% of Germs*

15 Wipes

7.08 in x 4.72 in (18 cm x 12 cm)

NDC: 79827-101-15

INGREDIENTS AND APPEARANCE

SWET PROTECT 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79827-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	2.4336 mg

Inactive Ingredients
Ingredient Name	Strength
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
SODIUM BENZOATE (UNII: OJ245FE5EU)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
2-METHYL-2-METHYLAMINO-1-PROPANOL (UNII: UHE79J5KHU)
HONEY (UNII: Y9H1V576FH)
CARBOMER 940 (UNII: 4Q93RCW27E)
OAT (UNII: Z6J799EAJK)
POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79827-101-12	15 in 1 BAG; Type 0: Not a Combination Product	10/12/2020
2	NDC: 79827-101-20	140 in 1 CANISTER; Type 0: Not a Combination Product	10/12/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/18/2020

Labeler - Energía 5 Mas 1 Comercio, S.A. de C.V. (814860128)

Registrant - L Squared Global (117528076)