AIR AND WATER HAND SANITIZER - CHRISTMAS BERRY- ethyl alcohol gel

Air and Water by

Drug Labeling and Warnings

Air and Water by is a Otc medication manufactured, distributed, or labeled by Pearl World Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl Alcohol 70%

Purpose

Antiseptic

Uses

To decrease bacteria on the skin that could cause disease. When water, soap and towel are not available. Recommended for repeated use.

Warnings

For external use only: hands.

Flammable. Keep away from fire or flame.

When using this product Keep out of eyes, ears, or mouth. In case of eye contact, flush eyes thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.

Stop use and ask a doctor if Redness or irritation develop. Condition persists for more than 72 hours.

Keep out of reach of children. Children should be supervised by an adult when using this product. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions Wet hands thoroughly with product and allow to dry without wiping. No rinsing required. For children under 6, use only under adult supervision. Not recommended for infants.

STORAGE AND HANDLING

Other information Store below 105°F (40°C). May discolor certain fabrics. Harmful to wood finishes & plastics.

INACTIVE INGREDIENT

Inactive ingredients: Water (Aqua), Triethanolamine, Carbomer, Aloe Barbadensis Leaf Extract, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate (Vitamin E). Main Contain: FD & C Red 40 (CI 16035), FD & C Yellow 6 (CI 15985), FD & C Violet 2 (CI 60725), FD & C Blue 1 (CI 42090), FD & C Yellow 5 (CI 19140), FD & C Red 33(CI 17200).

SPL UNCLASSIFIED SECTION

70% Alcohol

Manufactured for and distributed by Pearl world Inc, NY, NY 10019
Pearlworldinc.com All rights reserved. Designed in the USA. Made in PRC.

Packaging

INGREDIENTS AND APPEARANCE

AIR AND WATER  HAND SANITIZER - CHRISTMAS BERRY
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69933-403
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
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
D&C VIOLET NO. 2 (UNII: 350KA7O6HK)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69933-403-50	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	09/17/2020
2	NDC: 69933-403-60	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/17/2020

Labeler - Pearl World Inc. (043130142)