SODIUM HYDROXIDE

Manufacturer: Gordon Laboratories
Effective date: 2010-07-16
Label type: HUMAN PRESCRIPTION DRUG LABEL
Version: 11
Source: legacy-cache
Hydrated at: 2026-08-02 01:51:47

Label at a glance#

ProductSODIUM HYDROXIDE

Active ingredientSODIUM HYDROXIDE

Label structure7 sections

Label contents#

Full prescribing information#

DESCRIPTION SECTION

Sodium Hydroxide Solution 10%, Purified Water

HOW SUPPLIED SECTION

Sodium Hydroxide Solution 10% is supplied in a 2 oz. amber glass bottle.

INDICATIONS & USAGE SECTION

Used to destroy or kill the mail matrix (matrixectomies). Sodium Hydroxide 10% forms a strongly alkaline and caustic solution. As a caustic agent, it is used to destroy organic tissue by chemical action.

Use two 10 second applications. NaOH must be neutralized with 5%

WARNINGS AND PRECAUTIONS SECTION

Enter section text here

For external use only. Harmful if taken internally. For Physician use only. May cause skin irritation. Do not get in eyes, on skin, or on clothing. In case of contact, immediately flush skin or eyes with plenty of water for at least 15 minutes. Contact a Physician. Keep out of reach of children.

SPL UNCLASSIFIED SECTION

Federal law prohibits dispensing without prescription. Physician use only.

SPL UNCLASSIFIED SECTION

Enter section text here

Store at room temperature 59-86 F(15-30C)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
10481-3006-1	2021-11-10	C162847	48780-1	960f7f55-c7e5-8e05-e053-dbdaa90a074a	SODIUM HYDROXIDE
10481-3006-1	2019-10-29	C162847	48780-1	960f7f55-c7e5-8e05-e053-dbdaa90a074a	SODIUM HYDROXIDE

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
10481-3006-1	ML - Milliliter	10481-3006	c2ea05fd-b088-49a2-bfbf-06b17b463ff6	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
SODIUM HYDROXIDE	ACTIVE INGREDIENT	55X04QC32I	11
SODIUM CATION	ACTIVE MOIETY	LYR4M0NH37	11
Water	INACTIVE INGREDIENT	059QF0KO0R	11

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

SODIUM HYDROXIDE
SODIUM CATION
Water

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
10481-3006	10481-3006-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SODIUM HYDROXIDE	55X04QC32I	ACTIB
Water	059QF0KO0R	IACT

Source Document#

Source XML · Source PDF

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
d04ea775-2ade-a506-e053-2a95a90a8352			cb72936e-d185-4e18-8d59-01d07098c46b	2021-11-08	Warnings	Exact identifier spl set id: cb72936e-d185-4e18-8d59-01d07098c46b

Reported adverse events (FAERS/openFDA)#

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