Sanidry

Manufacturer: QUIMICA ROSMAR S.A DE C.V
Effective date: 2021-01-18
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:37:09

Label at a glance#

ProductSanidry

Active ingredientHYDROGEN PEROXIDE

Label structure13 sections

Dosage and administration

Clean the affected area Remove wipes Rub together briskly until dry No rinsing required Do not reuse the towel, dispose immediately after use.

Storage and handling

Do not apply internally Store at temperature below 110F(43C) Hold away from face when opening

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

This is a hand sanitizer manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19); Guidance for Industry.

The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:

Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (80%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
Glycerol (1.45% v/v).
Hydrogen peroxide (0.125% v/v).
Sterile distilled water or boiled cold water.

The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Hydrogen peroxide 3% v/v. Purpose: First Aid Antiseptic

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Use

INDICATIONS & USAGE SECTION

As an antiseptic to help prevent infection in minor cuts, scrapes, burns.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

Do not use in the eyes or apply over large areas of the body

Ask a doctor before use if you have deep or puncture wounds, animal bites or serious burns.

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use

if the condition persists or gets worse
irritation, pain or redness persists or worsens
swelling, rash or fever develops

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Clean the affected area
Remove wipes
Rub together briskly until dry
No rinsing required
Do not reuse the towel, dispose immediately after use.

Other information

STORAGE AND HANDLING SECTION

Do not apply internally
Store at temperature below 110F(43C)
Hold away from face when opening

Inactive ingredients

INACTIVE INGREDIENT SECTION

purified water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

300 units NDC: 77251-007-01 Package Label. Principal Display Panel.-000-00

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
797811	hydrogen peroxide 3 % Medicated Pad	PSN	2
797811	hydrogen peroxide 30 MG/ML Medicated Pad	SCD	2
797811	hydrogen peroxide 3 % Medicated Pad	SY	2
797811	hydrogen peroxide 3 % Topical Swab	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
77251-007-01	2024-01-30	C162847	48780-1	1030e365-1a38-111a-e063-dadaa90a10e2	77251-007 Sanidry Hydrogen Peroxide 3%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
77251-007-01	Sanidry	1275 mL in 1 BAG	CLOTH	1275		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
77251-007	SANIDRY (ALCOHOL) CLOTH [QUIMICA ROSMAR S.A DE C.V]	2	Legacy NDC, 1 package rows	20210121_b8411e12-39df-b099-e053-2a95a90a3b66.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Sanidry
ALCOHOL
HYDROGEN PEROXIDE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
77251-007	77251-007-01

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
HYDROGEN PEROXIDE	BBX060AN9V	ACTIB
WATER	059QF0KO0R	IACT

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
b9354c76-ef51-650e-e053-2995a90a8300			b8411e12-39df-b099-e053-2a95a90a3b66	2021-01-18	Warnings	Exact identifier spl id: b9354c76-ef51-650e-e053-2995a90a8300 spl set id: b8411e12-39df-b099-e053-2a95a90a3b66

Reported adverse events (FAERS/openFDA)#

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