NGA ALCOHOL WIPES SANDSTONE

Manufacturer
NEVER GO ALONE
Effective date
2023-10-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:56:38

Label at a glance#

ProductNGA ALCOHOL WIPES SANDSTONE
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

How to Use: insert pack into case, remove sticker. Dispense one wipe. WIpe hands thoroughly including between fingers & around fingerails. Allow to air dry. Dispense one wipe. Wipe hands thoroughly including between fingers & around fingernails. Allow to Air dry.

Storage and handling

Store below 104°F(40°C). Each wipe is 15 x 12 cm. May discolour certain fabrics. Do not use as a baby wipe, on the face, or in the intimate area. Made in UK for Never Go Alone Ltd.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Hand sanitizer (65%(w/w) denatured ethanol in an aqueous solution):

- Manufactured using United States Pharmacopoeia (USP) grade ingredients including USP water.

- The alcohol (ethanol) is (USP or Food Chemical Codex (FCC) grade), and is denatured according to Alcohol & Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.

OTC - ACTIVE INGREDIENT SECTION

Ethanol Alcohol 65%

OTC - PURPOSE SECTION

Antiseptic

USES

OTC - PURPOSE SECTION

Uses: Reducing Bacteria on skin

WARNINGS SECTION

Flammable. Keep away from fire and flame. External use only. Do not use in eyes. If contact occurs, flush thoroughly with water. Stop use and ask doctor if redness or irritation develops and continues for more than 72 hours. Keep out of reach of children. If swallowed, get medical help or contact the poison control centre immediately.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

INDICATIONS & USAGE SECTION

How to Use: insert pack into case, remove sticker. Dispense one wipe. WIpe hands thoroughly including between fingers & around fingerails. Allow to air dry.

DOSAGE & ADMINISTRATION SECTION

Dispense one wipe. Wipe hands thoroughly including between fingers & around fingernails. Allow to Air dry.

Other Information

STORAGE AND HANDLING SECTION

Store below 104°F(40°C). Each wipe is 15 x 12 cm. May discolour certain fabrics. Do not use as a baby wipe, on the face, or in the intimate area. Made in UK for Never Go Alone Ltd.

INACTIVE INGREDIENT SECTION

AQUA, ALOE VERA EXTRACT (ALOE BARDANENSIS WATER), GLYCERIN, CERAMIDE 2, GREEN TEA LEAF EXTRACT, CALENDULA, CHAMOMILE, GINSENG EXTRACT, FRAGRANCE (PARFUM)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

10 wipes; 83732-0110-1 10 Wipes - SANDSTONE PACKET10 Wipes - SANDSTONE PACKET

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
884787ethanol 65 % Medicated PadPSN1
884787ethanol 0.65 ML/ML Medicated PadSCD1
884787ethanol 65 % Medicated PadSY1
884787ethyl alcohol 65 % WipesSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83732-0110-12025-01-30C16284748780-12cef2736-7ed5-d83d-e063-dadaa90ab31fNEVER GO ALONE - HAND WIPES - EDITION 01 : SANDSTONE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83732-0110-1NGA ALCOHOL WIPES SANDSTONE27 g in 1 PACKETSWAB271

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83732-0110NGA ALCOHOL WIPES SANDSTONE (ETHANOL) SWAB [NEVER GO ALONE]11 package rows20231013_06f91e45-38a0-235c-e063-6294a90afbe6.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83732-011083732-0110-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
06f91e45-38a1-235c-e063-6294a90afbe606f91e45-38a0-235c-e063-6294a90afbe62023-10-05WarningsExact identifier
spl id: 06f91e45-38a1-235c-e063-6294a90afbe6
spl set id: 06f91e45-38a0-235c-e063-6294a90afbe6

Reported adverse events (FAERS/openFDA)#

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