Shit in the Woods Hand Sanitizer

Manufacturer: Blue Q
Effective date: 2023-01-02
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 21:41:44

Label at a glance#

ProductShit in the Woods Hand Sanitizer

Active ingredientALCOHOL

Label structure12 sections

Indications and uses

For handwashing to decrease bacteria on the skin.

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic Handwash

Uses

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from fire and flame.

When using this product

OTC - WHEN USING SECTION

When using this product do not use in the eyes. In case of contact with eyes, rinse eyes with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develops and persists.

Keep out of reach of children

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping.

Other information

OTHER SAFETY INFORMATION

Store under 105°F

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), vegetable glycerin, isopropyl myristate, aloe vera, carbomer, fragrance

SPL UNCLASSIFIED SECTION

I Just Shit in the Woods™

HAND SANITIZER

2 fl oz (59 ml)

Manufactured for Blue Q

703 West Housatonic t.

Pittsfield, MA 01201

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

back label

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Shit in the Woods Hand Sanitizer
Alcohol
WATER
GLYCERIN
ISOPROPYL MYRISTATE
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
ALOE VERA LEAF

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
65194-624	65194-624-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
ISOPROPYL MYRISTATE	0RE8K4LNJS	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
ALOE VERA LEAF	ZY81Z83H0X	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
eff7f3e3-ca39-3967-e053-2995a90a30db			a73682c0-cfe8-d6fd-e053-2995a90a3eab	2023-01-02	Warnings	Exact identifier spl id: eff7f3e3-ca39-3967-e053-2995a90a30db spl set id: a73682c0-cfe8-d6fd-e053-2995a90a3eab

Reported adverse events (FAERS/openFDA)#

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