Peppermint Aqua

Manufacturer
Double Rider Medicine Co., Ltd.
Effective date
2020-04-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:08:09

Label at a glance#

ProductPeppermint Aqua
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

Take a few drops. Apply directly on the skin or sprinkle to the surrounding environment when you are tired from class, meeting, driving, traveling and camping. Relieve itching with it when you are bitten by mosquitoes. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Peppermint Aqua

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. Purpose: Antiseptic, Fresh-up and Cool-down

Purpose

OTC - PURPOSE SECTION

Shuangfeiren Peppermint Aqua

Used for: refreshing, cooling, cleaning, anti-mosquito, relieve itching, class, meeting, traveling, camping, home.

mild nature, fragrant smell

Use

INDICATIONS & USAGE SECTION

Apply directly on the skin or sprinkle to the surrounding environment.

Fresh-up with it when you are tired from class, meeting, driving, traveling and camping. Relieve itching with it when you are bitten by mosquitoes.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Take a few drops. Apply directly on the skin or sprinkle to the surrounding environment when you are tired from class, meeting, driving, traveling and camping. Relieve itching with it when you are bitten by mosquitoes.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION


AQUA
MENTHA HAPLOCALYX OIL

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

202050506060packagepackage

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2286295ethanol 75 % Topical SprayPSN1
2286295ethanol 0.75 ML/ML Topical SpraySCD1
2286295ethanol 75 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76845-101-012021-07-23C16284748780-1c7ccaba7-1e4b-fd44-e053-dadaa90aa01bPeppermint Aqua
76845-101-022021-07-23C16284748780-1c7ccaba7-1e4b-fd44-e053-dadaa90aa01bPeppermint Aqua
76845-101-032021-07-23C16284748780-1c7ccaba7-1e4b-fd44-e053-dadaa90aa01bPeppermint Aqua

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76845-101-01Peppermint Aqua20 mL in 1 BOTTLELIQUID201
76845-101-02Peppermint Aqua50 mL in 1 BOTTLELIQUID501
76845-101-03Peppermint Aqua60 mL in 1 BOTTLELIQUID601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76845-101PEPPERMINT AQUA (ALCOHOL) LIQUID [DOUBLE RIDER MEDICINE CO., LTD.]1Legacy NDC, 3 package rows20200427_a43c9926-5022-34bf-e053-2a95a90acdfc.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76845-10176845-101-01, 76845-101-02, 76845-101-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHA ARVENSIS LEAF OIL1AEY1M553NIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML · Source PDF

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
a43c9926-5014-34bf-e053-2a95a90acdfca43c9926-5022-34bf-e053-2a95a90acdfc2020-04-26WarningsExact identifier
spl id: a43c9926-5014-34bf-e053-2a95a90acdfc
spl set id: a43c9926-5022-34bf-e053-2a95a90acdfc

Reported adverse events (FAERS/openFDA)#

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