Rise Hand Sanitizer by Shop Safely, LLC. Rise Hand Sanitizer

Rise Hand Sanitizer by

Drug Labeling and Warnings

Rise Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Shop Safely, LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

RISE HAND SANITIZER- ethyl alcohol gel 
Shop Safely, LLC.

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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Rise Hand Sanitizer

Active ingredient[s]:

Ethyl Alcohol 63% v/v

Purpose

Antiseptic

Use[s]

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammable. Keep away from heat or flame

Do not use

• in children less than 2 months of age
• on open skin wound or on broken skin

When using this product

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222

Directions

• Pump enough product on palms to cover hands. Rub hands together until dry.
• Children under 6 years of age should be supervised when using this product.

Other Information

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

aminomethyl propanol, carbomer, fragrance, glycerin, water.

PACKAGE/LABEL PRINCIPAL DISPLAY PANEL

Safely™
Hand Sanitizer

Rise

16 fl oz (1 pt) 473 mL

Manufactured for Shop Safely, LLC.
SAFELY™ and other trademarks owned by
Shop Safely, LLC. All rights reserved.
safelyclean.com
(888) 6-SAFELY
3578 Hayden Ave, Culver City, CA 90232

Made in the USA with US and imported
components This bottle is made with 10% PCR

Label

RISE HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81151-102
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	63 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81151-102-01	437 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/01/2021	06/30/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/01/2021	06/30/2024

Labeler - Shop Safely, LLC. (117715242)

Revised: 3/2022

Document Id: 41eeeb9d-1e56-4df4-9130-298271847c48

34390-5

Set id: bda5017f-3c56-4f33-a98d-f1e38e4af9d3

Version: 2

Effective Time: 20220309