Search by Drug Name or NDC

NDC 00363-0952-16 Advanced Hand Sanitizer 700 mg/mL Details

Advanced Hand Sanitizer 700 mg/mL

Advanced Hand Sanitizer is a TOPICAL GEL in the HUMAN OTC DRUG category. It is labeled and distributed by Walgreen Co. The primary component is ALCOHOL.

Product Information

NDC	00363-0952
Product ID	0363-0952_1493a2b0-f001-4485-ac97-639234d190e7
Associated GPIs	86209902904220
GCN Sequence Number	065933
GCN Sequence Number Description	mineral oil/petrolatum,white OINT. (G) 42.5-57.3% OPHTHALMIC
HIC3	Q6Y
HIC3 Description	EYE PREPARATIONS, MISCELLANEOUS (OTC)
GCN	28068
HICL Sequence Number	002215
HICL Sequence Number Description	MINERAL OIL/PETROLATUM,WHITE
Brand/Generic	Generic
Proprietary Name	Advanced Hand Sanitizer
Proprietary Name Suffix	n/a
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	Walgreen Co
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH NOT FINAL
Application Number	part333A
Listing Certified Through	2024-12-31

Package

Package Images

NDC 00363-0952-16 (00363095216)

Pricing Information	N/A
NDC Package Code	0363-0952-16
Billing NDC	00363095216
Package	59 mL in 1 BOTTLE, DISPENSING (0363-0952-16)
Marketing Start Date	2013-03-21
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL ed7e0cee-5a55-4e05-84d0-e5d09e20523b Details

Active ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

Uses

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

Warnings

For external use only-hands

Flammable. Keep away from heat and flame.

When using this product

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

Stop use and ask a doctor if

irritation or redness develops
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 105⁰ F
may discolor some fabrics
harmful to wood finishes and plastics

Inactive ingredients

water, aloe barbadensis leaf juice, glyceryl caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, benzophenone-4, blue 1, yellow 5

Questions?

1-888-593-0593

SPL UNCLASSIFIED SECTION

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

**This product is not manufactured or distributed by GOJO Industries, Inc. distributor of Purell Refreshing Aloe Advanced Hand Sanitizer.

Made in the U.S.A. and with U.S. and foreign components

DISTRIBUTED BY:

WALGREEN CO.,

200 WILMOT RD., DEERFIELD, IL 60015

100% SATISFACTION GUARANTEED walgreens.com

principal display panel

Well at Walgreens

WALGREENS PHARMACIST RECOMMENDED

Advanced Hand Sanitizer with Aloe

Leaves hands soft
Contains moisturizers & Vitamin E
Kills more than 99.99% of germs*

ALOE

Compare to Purell**

8 FL OZ (236 mL)

INGREDIENTS AND APPEARANCE

ADVANCED HAND SANITIZER

ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0363-0952
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)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
SULISOBENZONE (UNII: 1W6L629B4K)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:0363-0952-16	59 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	03/21/2013
2	NDC:0363-0952-34	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/21/2013

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	03/21/2013

Labeler - Walgreen Co (008965063)

Registrant - Vi-Jon, LLC (790752542)

Name	Address	ID/FEI	Business Operations
Establishment
Vi-Jon, LLC		088520668	manufacture(0363-0952)

Name	Address	ID/FEI	Business Operations
Establishment
Vi-Jon, LLC		790752542	manufacture(0363-0952)

Revised: 3/2022

Document Id: 1493a2b0-f001-4485-ac97-639234d190e7

Set id: ed7e0cee-5a55-4e05-84d0-e5d09e20523b

Version: 10

Effective Time: 20220307