FDA.reportPublic FDA data

Double Prawn Brand Herbal Oil

Manufacturer
Tai Tong Ah Co Pte Ltd
Effective date
2013-11-11
Label type
HUMAN OTC DRUG LABEL
Version
2993
Source
full-release
Hydrated at
2026-05-31 22:37:25

Label at a glance#

ProductDouble Prawn Brand Herbal Oil
Active ingredientMENTHOL
Label structure11 sections

Dosage and administration

Apply Herbal Oil to the affective area several times; use cotton dressing if necessary, repeat several times until completely healed.

Storage and handling

Store at cool and dry place from direct sunlight.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Menthol 3.5%

PURPOSE

OTC - PURPOSE SECTION

Menthol   External Analgesic

USE

INDICATIONS & USAGE SECTION

For the relief from pain, swelling and itching due to skin irritation, skin infection, minor cuts, fungal infection, abrasions, bruises, minor burns and scalds, insect bites and a range of skin problems.

WARNING

WARNINGS SECTION

For external use only and use as directed. Avoid contact with eyes, mucous membrances or rashes, wounds or damage skin. Do not use with a heated pad.

WARNING

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help immediately.

WARNING

OTC - STOP USE SECTION

Stop use and consult a doctor if excessive irritaion of the skin develops. For children under 2 years of age, consult a doctor.

DIRECTIONS

INSTRUCTIONS FOR USE SECTION

Apply Herbal Oil to the affective area several times; use cotton dressing if necessary, repeat several times until completely healed.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Apply Herbal Oil several times daily.

STORAGE

STORAGE AND HANDLING SECTION

Store at cool and dry place from direct sunlight.

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Camphor, dictampus dasycarpus, commiphora myrrha, sophora flavescens, sanguisorba officinalis, gleditsia sinensis, rheum palamatum

DRUG FACTS

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DRUG FACTSDRUG FACTS

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1442685menthol 3.5 % Topical OilPSN2993
1442685menthol 35 MG/ML Topical OilSCD2993
1442685menthol 3.5 % Topical OilSY2993

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
14720-372-302019-11-27C16284748780-19855e2a2-389d-60a7-e053-dbdaa90a05bdDouble Prawn Brand Herbal Oil

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
14720-372-29Double Prawn Brand Herbal Oil28 mL in 1 BOTTLE, GLASSOIL282993
14720-372-30Double Prawn Brand Herbal Oil1 in 1 CARTONOIL12993

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
14720-372DOUBLE PRAWN BRAND HERBAL OIL (BENZOCAINE, MENTHOL) OIL [TAI TONG AH CO PTE LTD]2993Legacy NDC, 2 package rows20131112_9c31740f-3dd3-4b0c-8b15-75a28af01f00.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
MENTHOLACTIVE INGREDIENTL7T10EIP3A2993
MENTHOLACTIVE MOIETYL7T10EIP3A2993
CAMPHOR (SYNTHETIC)INACTIVE INGREDIENT5TJD82A1ET2993
COMMIPHORA MYRRHA WHOLEINACTIVE INGREDIENTUU81N77RI72993
DICTAMNUS DASYCARPUS WHOLEINACTIVE INGREDIENTIM7ZCU30YH2993
GLEDITSIA SINENSIS WHOLEINACTIVE INGREDIENTFS3UB95UTG2993
RHEUM PALMATUM WHOLEINACTIVE INGREDIENT75P857ARCY2993
SANGUISORBA OFFICINALIS WHOLEINACTIVE INGREDIENTJ578M57Q8Z2993
SOPHORA FLAVESCENS WHOLEINACTIVE INGREDIENTX8KX602M5L2993

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
14720-37214720-372-29, 14720-372-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOLL7T10EIP3AACTIB
CAMPHOR (SYNTHETIC)5TJD82A1ETIACT
DICTAMNUS DASYCARPUS WHOLEIM7ZCU30YHIACT
COMMIPHORA MYRRHA WHOLEUU81N77RI7IACT
SOPHORA FLAVESCENS WHOLEX8KX602M5LIACT
SANGUISORBA OFFICINALIS WHOLEJ578M57Q8ZIACT
GLEDITSIA SINENSIS WHOLEFS3UB95UTGIACT
RHEUM PALMATUM WHOLE75P857ARCYIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
CAMPHOR (SYNTHETIC)CAMPHOR (SYNTHETIC)5TJD82A1ETDROPS / OPHTHALMICNAExact identifier — unii candidate
2 equally ranked IID candidates
CAMPHOR (SYNTHETIC)CAMPHOR (SYNTHETIC)5TJD82A1ETJELLY / NASAL65 mgExact identifier — unii candidate
2 equally ranked IID candidates

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
53601099-5e12-4e1a-82dc-2fc3f08128fa9c31740f-3dd3-4b0c-8b15-75a28af01f002013-11-11WarningsExact identifier
spl id: 53601099-5e12-4e1a-82dc-2fc3f08128fa
spl set id: 9c31740f-3dd3-4b0c-8b15-75a28af01f00

Reported adverse events (FAERS/openFDA)#

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