Forest sup

Manufacturer: our tree co.ltd | GOOD NATURE CO.,LTD
Effective date: 2020-06-25
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:19:01

Label at a glance#

ProductForest sup

Active ingredientALCOHOL

Label structure8 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping

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 65%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

To decrease bacteria on skin

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Other information

STORAGE AND HANDLING SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Cypress Water, Cypress Essence Oil

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
902515	ethanol 65 % Topical Spray	PSN	1
902515	ethanol 0.65 ML/ML Topical Spray	SCD	1
902515	ethanol 65 % Topical Spray	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
78799-001-01	2021-07-23	C162847	48780-1	c7ccaba7-20af-fd44-e053-dadaa90aa01b	78799-001_Forest sup
78799-001-02	2021-07-23	C162847	48780-1	c7ccaba7-20af-fd44-e053-dadaa90aa01b	78799-001_Forest sup
78799-001-03	2021-07-23	C162847	48780-1	c7ccaba7-20af-fd44-e053-dadaa90aa01b	78799-001_Forest sup
78799-001-04	2021-07-23	C162847	48780-1	c7ccaba7-20af-fd44-e053-dadaa90aa01b	78799-001_Forest sup
78799-001-05	2021-07-23	C162847	48780-1	c7ccaba7-20af-fd44-e053-dadaa90aa01b	78799-001_Forest sup
78799-001-06	2021-07-23	C162847	48780-1	c7ccaba7-20af-fd44-e053-dadaa90aa01b	78799-001_Forest sup

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
78799-001-01	Forest sup	60 mL in 1 BOTTLE, SPRAY	SPRAY	60	1
78799-001-02	Forest sup	300 mL in 1 BOTTLE, SPRAY	SPRAY	300	1
78799-001-03	Forest sup	500 mL in 1 BOTTLE, SPRAY	SPRAY	500	1
78799-001-04	Forest sup	1000 mL in 1 CONTAINER	SPRAY	1000	1
78799-001-05	Forest sup	5000 mL in 1 CONTAINER	SPRAY	5000	1
78799-001-06	Forest sup	20000 mL in 1 CONTAINER	SPRAY	20000	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78799-001	FOREST SUP (ALCOHOL) SPRAY [OUR TREE CO.LTD]	1	Legacy NDC, 6 package rows	20200626_780eba70-b227-4347-bb06-31a14c54d4df.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Forest sup
alcohol
WATER
GLYCERIN
CHAMAECYPARIS OBTUSA WOOD OIL
CUPRESSUS SEMPERVIRENS LEAF OIL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78799-001	78799-001-01, 78799-001-02, 78799-001-03, 78799-001-04, 78799-001-05, 78799-001-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
CHAMAECYPARIS OBTUSA WOOD OIL	P2OMP71Y62	IACT
CUPRESSUS SEMPERVIRENS LEAF OIL	M7QUY89S4O	IACT
ALCOHOL	3K9958V90M	ACTIB

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
a8f1030d-3a87-068b-e053-2a95a90a5b50			780eba70-b227-4347-bb06-31a14c54d4df	2020-06-25	Warnings	Exact identifier spl id: a8f1030d-3a87-068b-e053-2a95a90a5b50 spl set id: 780eba70-b227-4347-bb06-31a14c54d4df

Reported adverse events (FAERS/openFDA)#

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