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NDC 11822-4813-02 Daylogic Advanced Hand Sanitizer 700 mg/mL Details

Daylogic Advanced Hand Sanitizer 700 mg/mL

Daylogic Advanced Hand Sanitizer is a TOPICAL GEL in the HUMAN OTC DRUG category. It is labeled and distributed by Rite Aid Corporation. The primary component is ALCOHOL.

Product Information

NDC	11822-4813
Product ID	11822-4813_e9ac92d0-0d32-4fb4-80bd-ecabe21c8d8d
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Daylogic Advanced Hand Sanitizer
Proprietary Name Suffix	Refill
Non-Proprietary Name	Ethyl Alcohol
Product Type	HUMAN OTC DRUG
Dosage Form	GEL
Route	TOPICAL
Active Ingredient Strength	700
Active Ingredient Units	mg/mL
Substance Name	ALCOHOL
Labeler Name	Rite Aid Corporation
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH NOT FINAL
Application Number	part333E
Listing Certified Through	2022-12-31

Package

Package Images

NDC 11822-4813-02 (11822481302)

Pricing Information	N/A
NDC Package Code	11822-4813-2
Billing NDC	11822481302
Package	946 mL in 1 BOTTLE, PLASTIC (11822-4813-2)
Marketing Start Date	2017-04-27
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 34f255cc-bf3d-470b-beda-4489fcae3b4f Details

Active ingredient

Ethyl Alcohol 70% (v/v)

Purpose

Antibacterial

Uses

to help reduce bacteria on the skin.

Warnings

For external use only

Flammable
Keep away from source of heat or fire

When using this product

avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if

irritation or redness develops and lasts.

Keep out of reach of children.

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

use only to refill a hand sanitizer pump bottle.
from the pump bottle, put enough product in your palm to cover hands and rub hands together until dry.
children under 6 years should be supervised when using this product.

Other information

store at a temperature below 110°F (43°C).
may discolor certain fabrics or surfaces.

Inactive ingredients

Water (Aqua), Isopropyl Alcohol, Glycerin, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Carbomer, Aminomethyl Propanol, Fragrance (Parfum).

Questions or comments?

1-866-695-3030

Label Copy

INGREDIENTS AND APPEARANCE

DAYLOGIC ADVANCED HAND SANITIZER REFILL

ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:11822-4813
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	700 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
CARBOMER 934 (UNII: Z135WT9208)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:11822-4813-2	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/27/2017

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	04/27/2017

Labeler - Rite Aid Corporation (014578892)

Registrant - Apollo Health and Beauty Care Inc. (201901209)

Name	Address	ID/FEI	Business Operations
Establishment
Apollo Health and Beauty Care Inc.		201901209	manufacture(11822-4813)

Revised: 4/2017

Document Id: e9ac92d0-0d32-4fb4-80bd-ecabe21c8d8d

Set id: 34f255cc-bf3d-470b-beda-4489fcae3b4f

Version: 1

Effective Time: 20170428