Daylogic 471.000/471AA Ocean Breeze Hand Sanitizer

Alcohol by

Drug Labeling and Warnings

Alcohol by is a Otc medication manufactured, distributed, or labeled by Rite Aid, Vi Jon, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ALCOHOL- alcohol liquid 
Rite Aid

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Daylogic 471.000/471AA
Ocean Breeze Hand Sanitizer

Active ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Use

• to decrease bacteria on the skin that could cause disease
• recommended for repeated use

Warnings

For exterenal use only-hands

Flammable, keep away from fire or flame.

When using this product

• keep out of eyes.  In case of contact with eyes, flush thoroghly with water.
• avoid contact with broken skin
• do not inhale or ingest

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 medical help or contact a Poison Control Center right away

Directions

• wet hands thoroughly with product and allow to dry without wiping
• for children under 6, use only under adult supervision
• not recommended for infants

Other information

• do not store above 105⁰F
• may discolor some fabrics
• harmful to wood finishes and plastics

inactive ingredients

water, carbomer, fragrance, glycerin, isopropyl myristate, blue 1

Questions?

Satisfaction quaranteed - For questions or comments please call 1-888-287-1915

DISTRIBUTED BY RITE AID, 30 HUNTER LANE

CAMP HILL, PA 17011

*Effective at eliminating 99.99% of many common harmful germs and bacteria in as little as 15 seconds.

Principal display panel

Daylogic Hand Sanitizer

kills 99.99% of germs*

Moisturizers leave hand feeling smooth

8 FL OZ (236 mL)

ALCOHOL 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11822-9471
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
WATER (UNII: 059QF0KO0R)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11822-9471-1	89 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/03/2020	01/28/2022
2	NDC: 11822-9471-2	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/03/2020	01/28/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	02/10/2019	01/28/2022

Labeler - Rite Aid (014578892)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(11822-9471)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(11822-9471)

Revised: 10/2024

Document Id: 24b3f449-48d3-6117-e063-6394a90a257c

34390-5

Set id: d97fafba-dcc2-4cec-ae09-315e2a068057

Version: 7

Effective Time: 20241017