Plus Brasept Alcocol Gel

Manufacturer: NEWDROP NORTH AMERICA LLC | ABC Compounding Co., Inc.
Effective date: 2025-11-20
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-06-01 01:17:30

Label at a glance#

ProductPlus Brasept Alcocol Gel

Active ingredientALCOHOL

Label structure10 sections

Label contents#

Full prescribing information#

Drug Facts Box OTC-Active Ingredient Section

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% b/v

Drug Facts Box OTC-Purpose Section

OTC - PURPOSE SECTION

Antiseptic

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

FLAMMABLE, keep away from fire and flames

For external use only

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

wet hands thoroughly with product and allow to dry without wiping

Drug Facts Box OTC-Inactive Ingredient Section

INACTIVE INGREDIENT SECTION

water, DMD hydantoin, diisopropylamine, carbomer, propylene glycol, tocopheryl acetate, aloe barbadensis, fragrance

Plus Brasept Alcocol Gel 6605 Drug Facts and Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Plus Bracept Alcohol Gel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	4
581662	ethanol 0.7 ML/ML Topical Gel	SCD	4
581662	ethanol 70 % Topical Gel	SY	4
581662	ethyl alcohol 70 % Topical Gel	SY	4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
83318-605-08	Plus Brasept Alcocol Gel	208200 mL in 1 DRUM	GEL	208200		4
83318-605-14	Plus Brasept Alcocol Gel	3785 mL in 1 BOTTLE, PLASTIC	GEL	3785		4

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

Plus Brasept Alcocol Gel
ALCOHOL
WATER
CARBOMER 934
PROPYLENE GLYCOL
ALOE VERA LEAF
.ALPHA.-TOCOPHEROL ACETATE, DL-
DIISOPROPYLAMINE
DMDM HYDANTOIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
83318-605	83318-605-14, 83318-605-08

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
CARBOMER 934	Z135WT9208	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
.ALPHA.-TOCOPHEROL ACETATE, DL-	WR1WPI7EW8	IACT
DIISOPROPYLAMINE	BR9JLI40NO	IACT
DMDM HYDANTOIN	BYR0546TOW	IACT
ALCOHOL	3K9958V90M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Plus Brasept Alcocol Gel	ALCOHOL	NEWDROP NORTH AMERICA LLC	f791c99c-5879-9ba2-e053-6394a90ad3c7	2025-11-20	Warnings	Exact identifier ndc (package): 83318-605-14 ndc (package): 83318-605-08 ndc (product): 83318-605 ndc11 (package): 83318060508 ndc11 (package): 83318060514 spl id: 440c5ac8-dc18-6db4-e063-6294a90a6f19 spl set id: f791c99c-5879-9ba2-e053-6394a90ad3c7

Reported adverse events (FAERS/openFDA)#

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