FDA.reportPublic FDA data

GRIZZLY CREEK NATURALS HAND SANITIZER

Manufacturer
BLACK BIRD POTENTIALS INC. | GRIZZLY CREEK FARMS, LLC
Effective date
2020-05-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:14:54

Label at a glance#

ProductGRIZZLY CREEK NATURALS HAND SANITIZER
Active ingredientISOPROPYL ALCOHOL
Label structure12 sections

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient Isopropyl Alcohol 99%

OTC - PURPOSE SECTION

Purpose Antiseptic

INDICATIONS & USAGE SECTION

Uses To decrease bacteria on the skin that could cause disease; Recommended for repeated use

WARNINGS SECTION

Warnings ● For external use only: hands ● Flammable, keep away from fire or flame

OTC - WHEN USING SECTION

● When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest

OTC - STOP USE SECTION

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

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if irritation and redness develop or condition 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.

DOSAGE & ADMINISTRATION SECTION

Directions Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult super-vision. Use of product not recommended for infants.

OTC - WHEN USING SECTION

Other information Do not store above 105ºF. May discolor some fabrics. Harmful to wood finishes and plastics.

INACTIVE INGREDIENT SECTION

Inactive ingredients water, fragrance, aloe vera juice, sodium benzoate, potassium sorbate, xanthan gum.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

227 mL NDC: 73816-101- 8 oz front label8 oz front label02

946 mL NDC: 73816-101-04 32oz hand sanitizer32oz hand sanitizer

227 mL NDC: 73816-101-02 8 oz back label8 oz back label

3.875 L NDC: 73816-101-03 1 gal label1 gal label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73816-101-022022-01-28C16284748780-1d6a99b39-a796-a426-e053-dadaa90af4c2a2cb1105-5c29-1b50-e053-2995a90a00b5
73816-101-032022-01-28C16284748780-1d6a99b39-a796-a426-e053-dadaa90af4c2a2cb1105-5c29-1b50-e053-2995a90a00b5
73816-101-042022-01-28C16284748780-1d6a99b39-a796-a426-e053-dadaa90af4c2a2cb1105-5c29-1b50-e053-2995a90a00b5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73816-101-02GRIZZLY CREEK NATURALS HAND SANITIZER227 mL in 1 BOTTLE, PLASTICLIQUID2272
73816-101-03GRIZZLY CREEK NATURALS HAND SANITIZER3632 mL in 1 JUGLIQUID36322
73816-101-04GRIZZLY CREEK NATURALS HAND SANITIZER32 mL in 1 BOTTLE, DISPENSINGLIQUID322

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73816-101GRIZZLY CREEK NATURALS HAND SANITIZER (ALCOHOL) LIQUID [BLACK BIRD POTENTIALS INC.]2Legacy NDC, 3 package rows20200528_a2cb1105-5c29-1b50-e053-2995a90a00b5.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73816-10173816-101-02, 73816-101-03, 73816-101-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM BENZOATEOJ245FE5EUIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
WATER059QF0KO0RIACT
VACCINIUM MYRTILLUS ANTHOCYANOSIDESR911H793SUIACT
ISOPROPYL ALCOHOLND2M416302ACTIB
XANTHAN GUMTTV12P4NEEIACT
ALOE ARBORESCENS LEAF09TD8L5SQVIACT

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
a6a625b4-0bb9-1c6a-e053-2a95a90a700aa2cb1105-5c29-1b50-e053-2995a90a00b52020-05-27WarningsExact identifier
spl id: a6a625b4-0bb9-1c6a-e053-2a95a90a700a
spl set id: a2cb1105-5c29-1b50-e053-2995a90a00b5

Reported adverse events (FAERS/openFDA)#

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