SQUEAKY AQUA HAND SANITIZING GEL- alcohol gel

Squeaky Aqua Hand Sanitizing Gel by

Drug Labeling and Warnings

Squeaky Aqua Hand Sanitizing Gel by is a Otc medication manufactured, distributed, or labeled by SUNRAYSIA ORGANICS PRIVATE LIMITED. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

ACTIVE INGREDIENT

Active Ingredient:- Total Alcohol 80%

PURPOSE

Purpose:- Antiseptic

INDICATIONS & USAGE

Use:- Hand Sanitizer To Decrease Bacteria On The Skin

DOSAGE & ADMINISTRATION

Directions:- Take Small Amounts Of Squeaky Hand Cleansing Gel In Your Palm And Briskly Rub Hands

Together Until Dry. Cover The Finger Tips And Nails To Effectively Clean The Hands.

INACTIVE INGREDIENT

Ingredients:- Total Alcohol 80%, Demineralised Water, Glycerine, Carbomer, Triethanolamine, Fragrance, Color

WARNINGS

Warning:- Flammable Gel. Keep Away From Fire. If Accidentally Introduced In Eyes, Flush With Water.

Not For Medicinal Use. For External Use Only.

Keep Out Of Reach Of Children.

SPL UNCLASSIFIED SECTION

The Organic Story

Gentle and Soft with refreshing aroma

Manufactured By:-

Sunraysia Organics Pvt. Ltd.

Plot No:- 152/2/1 E&H Vithoba Industry Estate,

Bramanwade, Tal.Sinnar 422102, Nashik, MH, INDIA.

Office Address:

426, Neo Corporate Plaza, Ramchandra Lane Ext,

Off Kapolewadi, Malad (W), Mumbai 400064. MH

www.sunraysia.in

Customer Care: 1800 274 9933

GMP

ISO14001

biocert Natural

Packaging

INGREDIENTS AND APPEARANCE

SQUEAKY AQUA HAND SANITIZING GEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80288-024
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80288-024-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/27/2020
2	NDC: 80288-024-02	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/27/2020
3	NDC: 80288-024-03	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/27/2020
4	NDC: 80288-024-04	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/27/2020
5	NDC: 80288-024-05	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/27/2020
6	NDC: 80288-024-06	5000 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/27/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/27/2020

Labeler - SUNRAYSIA ORGANICS PRIVATE LIMITED (857979554)

Establishment
Name	Address	ID/FEI	Business Operations
SUNRAYSIA ORGANICS PRIVATE LIMITED		857979554	manufacture(80288-024)