Germ Eliminator

Manufacturer
Davion, Inc | Brands International Corp.
Effective date
2023-05-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:54:53

Label at a glance#

ProductGerm Eliminator
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Apply small amount to hands rub hands together vigorously until dry supervise children in use of this product

Storage and handling

Store below 110°F (43° C) may discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

To reduce bacteria on the skin

WARNINGS SECTION

Flammable, Keep away from fire or flame.

​For external use only.

When using this product

OTC - WHEN USING SECTION

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

irritation or redness develops

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply small amount to hands
  • rub hands together vigorously until dry
  • supervise children in use of this product

Other information

STORAGE AND HANDLING SECTION

Store below 110°F (43° C)

may discolor certain fabrics or surfaces

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Isopropyl Alcohol, Glycerin, Carbomer, Aminomethyl Propanol, Fragrance, Propylene Glycol, Isopropyl Myristate, Aloe Barbadensis Leaf Juice (Aloe Vera), Tocopheryl Acetate (Vitamin E).

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

A SHOPRITE BRAND

paperbird

fresh scent

Advanced

Hand Sanitizer

quick drying formula

KILLS

MORE THAN

99.99%

OF GERMS

With moisturizers

Paraben & phthalate

free formula

NET 15 FL OZ

(443 mL)

hand sanitizerhand sanitizer

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42669-015-152025-01-30C16284748780-12cef2736-9c1a-d83d-e063-dadaa90ab31fDrug Facts

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
42669-01542669-015-15

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
fae30560-efb2-6209-e053-6394a90a7baffae36294-68b8-bf14-e053-6394a90aaacd2023-05-04WarningsExact identifier
spl id: fae30560-efb2-6209-e053-6394a90a7baf
spl set id: fae36294-68b8-bf14-e053-6394a90aaacd

Reported adverse events (FAERS/openFDA)#

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