OTC Medication Information: S GVD Phytoncide

S GVD PHYTONCIDE- quercus acutissima whole, chamaecyparis obtusa whole and cryptomeria japonica bark liquid
Infinite Solution Co.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

ACTIVE INGREDIENTS

Quercus Acutissima Whole 1.7%
Chamaecyparis Obtusa Whole 1.7%
Cryptomeria Japonica Bark 1.6%

INACTIVE INGREDIENT

Water

PURPOSE

ANTISEPTIC

WARNINGS

• For external use only
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Do not use
• in children less than 2 months of age
• on open skin wounds
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When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

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

Uses

Hand sanitizing to help reduce bacteria that potentially can cause disease.

Directions

Use to refill this Phytoncide into Spray Apparatus

Other Information

■ Read the directions and warnings before use
■ Store between 15-30℃(59-89℉)
■ Avoid freezing and excessive heat above 40℃(104 ℉)

Package Label 81744-010-02: S-GVD Phytoncide (200mL, Bottle)

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Package Label 81744-010-04: S-GVD Phytoncide (500mL, Bottle)

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S GVD PHYTONCIDE
quercus acutissima whole, chamaecyparis obtusa whole, cryptomeria japonica bark liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:81744-010
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
QUERCUS ACUTISSIMA WHOLE (QUERCUS ACUTISSIMA WHOLE) QUERCUS ACUTISSIMA WHOLE 1.7 g in 100 mL
CHAMAECYPARIS OBTUSA WHOLE (CHAMAECYPARIS OBTUSA WHOLE) CHAMAECYPARIS OBTUSA WHOLE 1.7 g in 100 mL
CRYPTOMERIA JAPONICA BARK (CRYPTOMERIA JAPONICA BARK) CRYPTOMERIA JAPONICA BARK 1.6 g in 100 mL
Inactive Ingredients
Ingredient Name Strength
Water
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:81744-010-02 1 BOTTLE in 1 CARTON contains a BOTTLE (81744-010-01)
1 NDC:81744-010-01 200 mL in 1 BOTTLE This package is contained within the CARTON (81744-010-02)
2 NDC:81744-010-04 1 BOTTLE in 1 CARTON contains a BOTTLE (81744-010-03)
2 NDC:81744-010-03 500 mL in 1 BOTTLE This package is contained within the CARTON (81744-010-04)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 03/01/2021
Labeler — Infinite Solution Co. (695502472)
Registrant — Infinite Solution Co. (695502472)
Establishment
Name Address ID/FEI Operations
Infinite Solution Co. 695502472 manufacture (81744-010)

Revised: 04/2021 Infinite Solution Co.

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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