North Woods D-Germ Hand Sanitizing Gel

Manufacturer
Superior Chemical Corporation
Effective date
2023-01-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:39:22

Label at a glance#

ProductNorth Woods D-Germ
Active ingredientALCOHOL
Label structure10 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Ethyl Alcohol 70% v/v

OTC - PURPOSE SECTION

Purpose

Antiseptic

INDICATIONS & USAGE SECTION

Uses

  • To decrease bacteria on the skin that potentially can cause disease.
  • Recommended for repeated use.

WARNINGS SECTION

Warnings

  • FLAMMABLE. Keep away from heat or flame.
  • For external use only.

OTC - WHEN USING SECTION

Keep out of eyes, ears or mouth. In case of eye contact, flush eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develop or if condtion persists for more than 72 hours.

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. Children should be supervised by an adult when using this product.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Apply sufficient amount of product to your palm to cover both hands.
  • Rub until dry.

OTHER SAFETY INFORMATION

Other information

May discolor certain fabrics and surfaces

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Juice, FD&C Blue No. 1, FD&C Yellow No. 5, Fragrance, Isopropyl Alcohol, PEG/PPG-18/18 Dimethicone, Triethanolamine, Vitamin E, Water.

SPL UNCLASSIFIED SECTION

Questions?

Call: 1-800-242-7694 or visit our website: www.northwoods.com

North Woods®

Sheboyan, WI 53081

NOT TESTED ON ANIMALS

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

North Woods

D-Germ

Instant Waterless Hand Sanitizing Gel

18 fl. oz.

Northwoods D-Gel FrontNorthwoods D-Gel Front

Products#

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53125-80253125-802-04, 53125-802-18

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
f279624b-b4fe-f422-e053-2995a90a8728badd0cad-0cb7-a38d-e053-2995a90a8a6f2023-01-02WarningsExact identifier
spl id: f279624b-b4fe-f422-e053-2995a90a8728
spl set id: badd0cad-0cb7-a38d-e053-2995a90a8a6f

Reported adverse events (FAERS/openFDA)#

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