Search by Drug Name or NDC

NDC 59779-0955-16 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 CVS Pharmacy, Inc. The primary component is ALCOHOL.

Product Information

NDC	59779-0955
Product ID	59779-955_095696df-a5c5-4a25-a2dd-40f749ed844e
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	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	CVS Pharmacy, Inc
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH NOT FINAL
Application Number	part333A
Listing Certified Through	2023-12-31

Package

Package Images

NDC 59779-0955-16 (59779095516)

Pricing Information	N/A
NDC Package Code	59779-955-16
Billing NDC	59779095516
Package	59 mL in 1 BOTTLE, DISPENSING (59779-955-16)
Marketing Start Date	2013-01-13
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 13441921-1360-4f32-a8f7-7d6a718875fb 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, glyceryl, caprylate/caprate, glycerin, tocopheryl acetate, aloe barbadensis leaf juice, isopropyl myristate, acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, benzophenone-4, blue 1, ext. violet2

SPL UNCLASSIFIED SECTION

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

Distributed by:

CVS Pharmacy, Inc

One CVS Drive

Woonsocket, RI 02895

CVS.com 1-800-shop-CVS

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

principal display planel

Sea mineral scent

Adanced formula hand sanitizer

*kills 99.99% of germs

fast & effective

moisturizing formula with vitamin E

leaves hand feeling soft

CVS/pharmacy

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:59779-955
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)
GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
SULISOBENZONE (UNII: 1W6L629B4K)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:59779-955-16	59 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	01/13/2013
2	NDC:59779-955-34	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/13/2013

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	01/13/2013

Labeler - CVS Pharmacy, Inc (062312574)

Registrant - Vi-Jon, LLC (790752542)

Name	Address	ID/FEI	Business Operations
Establishment
Vi-Jon, LLC		088520668	manufacture(59779-955)

Name	Address	ID/FEI	Business Operations
Establishment
Vi-Jon, LLC		790752542	manufacture(59779-955)

Revised: 6/2022

Document Id: 095696df-a5c5-4a25-a2dd-40f749ed844e

Set id: 13441921-1360-4f32-a8f7-7d6a718875fb

Version: 15

Effective Time: 20220624