FDA.reportPublic FDA data

NATUBASE 70 Pine Antibacterial Wet Wipes

Manufacturer
SY Global Inc
Effective date
2020-06-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:25:43

Label at a glance#

ProductNATUBASE 70 Pine Antibacterial Wet Wipes
Active ingredientALCOHOL, PINUS DENSIFLORA WHOLE
Label structure11 sections

Storage and handling

Be careful when handling the packaging edges as they are sharp. There is a risk of deterioration if you put the wipes back inside with contaminated hands. Be sure to keep the sticker or cap closed after use.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

ALCOHOL 70%

PINUS DENSIFLORA WHOLE (Pine Tree Extract) 0.4%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Inactive Ingredient

INACTIVE INGREDIENT SECTION

WATER (Purified Water), LAMINARIA JAPONICA (Kelp Extract), CHAMAECYPARIS OBTUSA WHOLE (Chamaecyparis Obtusa Extract)

Use

DOSAGE & ADMINISTRATION SECTION

Open the cap and peel front label slowly

Pull out wipes as needed

Use

INDICATIONS & USAGE SECTION

Close the cap after each use to prevent moisture loss

Caution

OTC - ASK DOCTOR SECTION

If any irritation develops, stop using and consult a doctor if necessary.

Caution

OTC - WHEN USING SECTION

Do not use on damaged skin and avoid using on open scars.

Caution

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Caution

WARNINGS SECTION

Keep in dry cool place, avoiding direct sunlight, heat and flame.

Caution

STORAGE AND HANDLING SECTION

Be careful when handling the packaging edges as they are sharp.
There is a risk of deterioration if you put the wipes back inside with contaminated hands.
Be sure to keep the sticker or cap closed after use.

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

290g NDC: 77200-070-60 Label 1290g NDC: 77200-070-60 Label 1

290g NDC: 77200-070-60 Label 2290g NDC: 77200-070-60 Label 2

290g NDC: 77200-070-60 Label 3290g NDC: 77200-070-60 Label 3

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77200-07077200-070-60

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
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
LAMINARIA JAPONICAWE98HW412BIACT
CHAMAECYPARIS OBTUSA WHOLE80ZNL1G5XYIACT
PINUS DENSIFLORA WHOLEU797H98B8YACTIB

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
b905fb67-87ae-b542-e053-2995a90a214ea7d0a5a6-7da9-3726-e053-2a95a90a079b2021-01-16WarningsExact identifier
spl set id: a7d0a5a6-7da9-3726-e053-2a95a90a079b

Reported adverse events (FAERS/openFDA)#

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