RIPCLEAR ANTISEPTIC HAND SANITIZER- isopropyl alcohol liquid

RIPCLEAR ANTISEPTIC HAND SANITIZER by

Drug Labeling and Warnings

RIPCLEAR ANTISEPTIC HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Rip Clear LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Isopropyl alcohol 75% v/v

Purpose

Antiseptic

INDICATIONS & USAGE

Uses hand sanitizer to decrease bacteria on the skin recommended for repeated use for use when soap and water are not available

Warnings

Flammable, keep away from fire/flame
For external use only

Do not use in children less than 2 months of age on open skin wounds

When using this product do not get into eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor if irritation and redness develop condition persists for more than 72 hours

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

DOSAGE & ADMINISTRATION

Directions wet hands thoroughly with product and allow to dry without wiping  supervise children under 6 years of age when using this product to avoid swallowing

Other information

store between 59-86°F (15-30°C) avoid freezing and excessive heat above 104°F (40°C)

Inactive ingredients

acrylates/c-10-30 alkyl acrylate crosspolymer, aloe vera leaf juice, aminomethylpropanol, FD&C Blue #1, FD&C Red #40, fragrance, glycerin, propylene glycol, propylparaben, water

QUESTIONS

Questions? +1-917-968-3098

You may also report serious side effects to this phone number.

Mon-Fri 9:00 AM - 5:00 PM

SPL UNCLASSIFIED SECTION

Topical solution

Liquid, Non-Gel

PROUDLY MADE IN USA

Manufactured by: Dynamic Labs Inc. 
30 Haynes Ct., Ronkonkoma, NY, USA 11779

(631) 231-7474

Packaging

INGREDIENTS AND APPEARANCE

RIPCLEAR ANTISEPTIC HAND SANITIZER 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80555-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C RED NO. 40 (UNII: WZB9127XOA)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	blue (Light blue)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80555-001-10	59.15 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/20/2020
2	NDC: 80555-001-20	236.6 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/20/2020
3	NDC: 80555-001-30	3800 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/20/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/20/2020

Labeler - Rip Clear LLC (079813108)