99 Plus Hand Sanitizer

Manufacturer
Momar Incorporated | ABC Compounding Co., Inc.
Effective date
2026-01-06
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:31:35

Label at a glance#

Product99 Plus Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Label contents#

Full prescribing information#

Drug Facts Box OTC-Active Ingredient Section

OTC - ACTIVE INGREDIENT SECTION

benzalkonium chloride USP 0.13%

Drug Facts Box OTC-Indications & Usage Section

INDICATIONS & USAGE SECTION

For hand-washing to decrease bacteria on the skin, only when water is not available

Drug Facts Box OTC-Warnings Section

WARNINGS SECTION

For external use only

Drug Facts Box OTC-Purpose Section

OTC - PURPOSE SECTION

Antiseptic

Drug Facts Box-OTC When Using Section

OTC - WHEN USING SECTION

do not get into eyes

if contact occurs, rinse eyes thoroughly with water

Drug Facts Box-OTC Stop Use Section

OTC - STOP USE SECTION

irritation and redness develop

Drug Facts Box-OTC Keep Out Of Reach Of Children Section

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away

Drug Facts Box-OTC Dosage & Administration Section

DOSAGE & ADMINISTRATION SECTION

press pump twice to deliver two squirts (about a quarter size) of foaming product onto the palm of your hand

rub hands together until dry

wash hands with soap and water at earliest opportunity

Drug Facts Box-OTC Inactive Ingredient Section

INACTIVE INGREDIENT SECTION

water, glycerine, dimethicone, DMDM hydantoin, iodopropynl butylcarbamate, methylchloroisothiazolinone, methylisothiazolinone, fragrance

99 Plus Instant Hand Sanitizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

product labelproduct label

99 Plus Instant Hand Sanitizer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1020365benzalkonium chloride 0.13 % Topical FoamPSN4
1020365benzalkonium chloride 1.3 MG/ML Topical FoamSCD4
1020365benzalkonium chloride 0.13 % Topical FoamSY4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63533-457-1099 Plus Hand Sanitizer1000 mL in 1 CARTRIDGELIQUID10004
63533-457-1299 Plus Hand Sanitizer1000 mL in 1 BAGLIQUID10004
63533-457-1499 Plus Hand Sanitizer3785 mL in 1 BOTTLE, PLASTICLIQUID37854
63533-457-1899 Plus Hand Sanitizer50 mL in 1 BOTTLE, PLASTICLIQUID504

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63533-45763533-457-10, 63533-457-18, 63533-457-14, 63533-457-12

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
99 Plus Hand SanitizerBENZEALKONIUM CHLORIDEMomar Incorporatedf972a8f1-c928-4e4b-a8dd-a2fb77052d212026-01-06WarningsExact identifier
ndc (package): 63533-457-18
ndc (package): 63533-457-12
ndc (package): 63533-457-14
ndc (package): 63533-457-10
ndc (product): 63533-457
ndc11 (package): 63533045714
ndc11 (package): 63533045718
ndc11 (package): 63533045710
ndc11 (package): 63533045712
spl id: 47b981ad-adb6-7ecb-e063-6394a90ac578
spl set id: f972a8f1-c928-4e4b-a8dd-a2fb77052d21

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.