SAFE CLEANER PLUS- alcohol liquid

SAFE CLEANER PLUS by

Drug Labeling and Warnings

SAFE CLEANER PLUS by is a Otc medication manufactured, distributed, or labeled by S-ONE PHARMACEUTICAL INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl alcohol 70%

Purpose

Antimicrobial

Uses

Hand sanitizer to help reduce bacteria on the skin.

Warnings

Flammable. Keep away from fire or flame.

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 appears and lasts.

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 Safe Cleaner Hand Sanitizer.

Other information

* Store below 110F (43C)

* May discolor certain fabrics or surfaces.

Inactive Ingredients

Glycerine, Purified water, Propylene glycol, Carbomer, Triethanolamine, Sophora extract, Grapefruit seed extract, Mentha oil

Package Label

INGREDIENTS AND APPEARANCE

SAFE CLEANER PLUS 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74721-0010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
TROLAMINE (UNII: 9O3K93S3TK)
SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
CITRUS PARADISI SEED (UNII: 12F08874Y7)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
PEPPERMINT OIL (UNII: AV092KU4JH)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74721-0010-4	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/24/2020
2	NDC: 74721-0010-5	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/24/2020
3	NDC: 74721-0010-6	475 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/24/2020
4	NDC: 74721-0010-7	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/24/2020
5	NDC: 74721-0010-8	2000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/24/2020
6	NDC: 74721-0010-9	4000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/24/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/24/2020

Labeler - S-ONE PHARMACEUTICAL INC (694626932)

Registrant - S-ONE PHARMACEUTICAL INC (694626932)

Establishment
Name	Address	ID/FEI	Business Operations
S-ONE PHARMACEUTICAL INC		694626932	manufacture(74721-0010)