PURIF Hand Sanitizer by A.D.S. Sales Co. Inc / Ming Fai Innovative Skin Care Lab Limited PURIF Hand Sanitizer

PURIF Hand Sanitizer by

Drug Labeling and Warnings

PURIF Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by A.D.S. Sales Co. Inc, Ming Fai Innovative Skin Care Lab Limited. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURIF HAND SANITIZER- alcohol gel 
A.D.S. Sales Co. Inc

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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PURIF Hand Sanitizer

Drug Facts

Active Ingredient

Ethyl Alcohol 72% (v/v)

Purpose

Antibacterial

Uses

• To help reduce bacteria on the skin.

Warnings

• For external use only.
• Flammable.
• Keep away from fire or flame.

When using this product

• Avoid contact with eyes.
• If contact occurs, rinse thoroughly with water.

Stop using and ask a doctor if

• Irritation or redness develops and lasts.

Keep out of reach of children

• In case of accidental ingestion, get medical help or contact a poison control center immediately. 

Directions

• Squeeze a significant amount in your palm and rub hands until fully dry.
• Rinse free.

Other information

• Store below 110°F (43°C).

Inactive ingredients

Aqua (Water), Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Hydrolyzed Jojoba Esters, Phenoxyethanol, Parfum (Fragrance),  Aminomethyl Propanol, Tocopherol, Glycine, Soja (Soybean) Oil, Aloe Barbadensis Leaf Juice, Citrus Aurantium Dulcis (Orange) Fruit Extract, Olea Europaea (Olive) Fruit Oil

Package Labeling: 50ml

Package Labeling: 320ml

Package Labeling:500ml

Package Labeling: 1L

Package Labeling: 177ml

PURIF HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79249-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.72 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
TOCOPHEROL (UNII: R0ZB2556P8)
GLYCINE (UNII: TE7660XO1C)
SOYBEAN OIL (UNII: 241ATL177A)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ORANGE (UNII: 5EVU04N5QU)
OLIVE OIL (UNII: 6UYK2W1W1E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79249-020-00	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2020	12/31/2022
2	NDC: 79249-020-01	320 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2020	12/31/2022
3	NDC: 79249-020-02	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2020	12/31/2022
4	NDC: 79249-020-03	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2020	12/31/2022
5	NDC: 79249-020-04	177 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2020	12/31/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/01/2020	12/31/2022

Labeler - A.D.S. Sales Co. Inc (051216828)

Establishment
Name	Address	ID/FEI	Business Operations
Ming Fai Innovative Skin Care Lab Limited		663304471	manufacture(79249-020)

Revised: 3/2023

Document Id: f7ab4292-1c57-416b-e053-6294a90a3b40

34390-5

Set id: 3ffa4ea7-9fc2-46d0-a7cc-66486c89e5b3

Version: 3

Effective Time: 20230324