100% PURE HAND SANITIZER- ethyl alcohol spray

100% Pure Hand Sanitizer by

Drug Labeling and Warnings

100% Pure Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Purity Cosmetics, Our Babylon LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses

For cleaning hands when water is not available to help reduce bacteria on the skin. Recommended for repeated use.

Warnings:

• ​For external use only.

STORAGE AND HANDLING

• Flammable, keep away from fire, sparks, and sources of ignition.
• Do not store above 104°F/40°C.

WHEN USING

• When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water.

KEEP OUT OF REACH OF CHILDREN

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

OTHER SAFETY INFORMATION

• Avoid contact with broken skin.

STOP USE

• Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.

Directions:

Spray directly on hands and rub in thoroughly. For children under 6, use adult supervision. Not recommended for infants.

Other Ingredients:

Glycerin, Aloe Barbadensis (Aloe Vera) Leaf Juice*, Melaleuca Alternifolia (Tea Tree) Leaf Oil *Organic Ingredient

Questions or Comments?

Call 1.415.814.9788 or visit www.100PercentPure.com

PRINCIPAL DISPLAY PANEL

100% Pure Hand Sanitizer Spray with Tea Tree and Aloe

NDC: 52667-010-01

1.7 fl oz / 50 ml

INGREDIENTS AND APPEARANCE

100% PURE HAND SANITIZER 
ethyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52667-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
TEA TREE OIL (UNII: VIF565UC2G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52667-010-01	50 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/22/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/22/2020

Labeler - Purity Cosmetics (055795259)

Registrant - Our Babylon LLC (105266218)

Establishment
Name	Address	ID/FEI	Business Operations
Our Babylon LLC		105266218	manufacture(52667-010)