Puri-Clean Advanced Hand Sanitizer

Puri-Clean by

Drug Labeling and Warnings

Puri-Clean by is a Otc medication manufactured, distributed, or labeled by Prime Enterprises. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURI-CLEAN ADVANCED HAND SANITIZER- ethyl alcohol gel 
Prime Enterprises

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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Puri-Clean Advanced Hand Sanitizer

Active Ingredient(s)

Ethyl Alcohol 70% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

For Hand washing to decrease bacteria on the skin.

Warnings

For external use only. Flammable. do not use near heat, flame, or while smoking.

When using this product keep out of eyes. if product gets into eyes, rinse with water to remove.Avoid contact with broken skin. Do not inhale or ingest.

Stop use and ask a doctor if rash or irritation develops and lasts.

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

Directions

• Wet hands thoroughly with product and allow to dry with out wiping.
• For children under 6, use only under adult supervision.

Other information

• Do not store above 104F
• May discolor some fabrics, wood finishes and plastics

Inactive ingredients

Aloe Barbadensis Leaf Juice, Aminomethyl Propanol, Carbomer, Glycerin, Isopropyl Myristate, Tocopherol, Water

Puri-clean Advanced Hand Sanitizer

PURI-CLEAN  ADVANCED HAND SANITIZER
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58443-0353
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
TOCOPHEROL (UNII: R0ZB2556P8)
GLYCERIN (UNII: PDC6A3C0OX)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
WATER (UNII: 059QF0KO0R)
CARBOMER 934 (UNII: Z135WT9208)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58443-0353-3	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/08/2020	05/31/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/08/2020	05/31/2022

Labeler - Prime Enterprises (101946028)

Registrant - Prime Enterprises (101946028)

Establishment
Name	Address	ID/FEI	Business Operations
Prime Enterprises		101946028	manufacture(58443-0353) , pack(58443-0353) , label(58443-0353) , analysis(58443-0353)

Revised: 4/2022

Document Id: dbe9c605-c5ff-2dee-e053-2995a90a6d42

34390-5

Set id: ae304c6a-b47f-c383-e053-2a95a90a8bee

Version: 2

Effective Time: 20220405