DR.OH PATCH

Manufacturer
YEPHARM
Effective date
2011-08-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:29:19

Key Label Information#

Active Ingredients And Purpose

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: CAMPHOR (NATURAL) 1.42%, MENTHOL 0.8%

OTC - PURPOSE SECTION

Purpose: Topical analgesic

Uses

INDICATIONS & USAGE SECTION

Indication and usage: Adults and children over 12 years - use only as directed. - do not use on children under 12 years of age. - use up to 8 hours, repeat once if necessary. - reseal pouch containing unused patches.

Warnings

WARNINGS SECTION

Warnings: For external use only.

OTC - DO NOT USE SECTION

Do not use if - you are allergic to fragrance. - you have asthma. - you are pregnant or breast-feeding.

Directions And Dosage

DOSAGE & ADMINISTRATION SECTION

Dosage and administration: Use up to 8 hours, repeat once if necessary.

Other Label Information

INACTIVE INGREDIENT SECTION

Inactive ingredients: Eucalyptus globulus leaf oil, Thymol, castor oil, dodecanal, citronellol, geraniol, citronellal, cymbopogon nardus oil, benzophenone, phenoxybenzene, benzyl benzoate

STORAGE AND HANDLING SECTION

Storage: Store in a cool and dry location out of direct sunlight.

OTC - QUESTIONS SECTION

Questions: Phone: 608-362-6915 E-mail: drohpatch@gmail.com

Label Images#

dr.oh patch cello pack
dr.oh patch cello pack

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1117074camphor 1.42 % / menthol 0.8 % Medicated PatchPSN2
1117078Dr. Oh 1.42 % / 0.8 % Medicated PatchPSN2
1117078camphor 0.0142 MG/MG / menthol 0.008 MG/MG Medicated Patch [Dr. Oh Patch]SBD2
1117074camphor 0.0142 MG/MG / menthol 0.008 MG/MG Medicated PatchSCD2
1117074camphor 1.42 % / menthol 0.8 % Medicated PatchSY2
1117078Dr. Oh (camphor 1.42 % / menthol 0.8 % ) Medicated PatchSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76163-010-012019-10-29C16284748780-1960f7f55-d745-8e05-e053-dbdaa90a074aDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76163-010-01DR.OH PATCH2000 mg in 1 CELLO PACKPATCH20002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76163-010DR.OH PATCH (CAMPHOR (NATURAL)) PATCH [YEPHARM]2Legacy NDC, 1 package rows20110826_48ea81bb-e5be-481e-982f-694b5d5cb06e.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CAMPHOR (NATURAL)ACTIVE INGREDIENTN20HL7Q9412
MENTHOLACTIVE INGREDIENTL7T10EIP3A2
CAMPHOR (NATURAL)ACTIVE MOIETYN20HL7Q9412
MENTHOLACTIVE MOIETYL7T10EIP3A2
.BETA.-CITRONELLOL, (R)-INACTIVE INGREDIENTP01OUT964K2
BENZOPHENONEINACTIVE INGREDIENT701M4TTV9O2
BENZYL BENZOATEINACTIVE INGREDIENTN863NB338G2
CASTOR OILINACTIVE INGREDIENTD5340Y2I9G2
CITRONELLA OILINACTIVE INGREDIENTQYO8Q067D02
CITRONELLALINACTIVE INGREDIENTQB99VZZ7GZ2
ETHYL ACETATEINACTIVE INGREDIENT76845O8NMZ2
EUCALYPTUS GLOBULUS LEAFINACTIVE INGREDIENTS546YLW6E62
GERANIOLINACTIVE INGREDIENTL837108USY2
THYMOLINACTIVE INGREDIENT3J50XA376E2

Products#

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76163-01076163-010-01

Ingredients#

Complete SPL Sections#

OTC - ACTIVE INGREDIENT SECTION

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: CAMPHOR (NATURAL) 1.42%, MENTHOL 0.8%

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT SECTION

Inactive ingredients: Eucalyptus globulus leaf oil, Thymol, castor oil, dodecanal, citronellol, geraniol, citronellal, cymbopogon nardus oil, benzophenone, phenoxybenzene, benzyl benzoate

OTC - PURPOSE SECTION

OTC - PURPOSE SECTION

Purpose: Topical analgesic

WARNINGS SECTION

WARNINGS SECTION

Warnings: For external use only.

OTC - WHEN USING SECTION

OTC - WHEN USING SECTION

When using this product - use only as directed. - do not bandage tightly or use with a heating pad. - do not use on irritated, wounded or damaged skin. - avoid contact with eye or mucous membranes.

OTC - DO NOT USE SECTION

OTC - DO NOT USE SECTION

Do not use if - you are allergic to fragrance. - you have asthma. - you are pregnant or breast-feeding.

OTC - STOP USE SECTION

OTC - STOP USE SECTION

Stop use if - condition worsens or symptoms persist for more than 7days. - redness is present. - irritation develops.

OTC - ASK DOCTOR SECTION

OTC - ASK DOCTOR SECTION

Ask a doctor if - condition worsens or symptoms persist for more than 7days. - redness is present. - irritation develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children: If patch is swallowed, get medical help or contact poison control center immediately.

INDICATIONS & USAGE SECTION

INDICATIONS & USAGE SECTION

Indication and usage: Adults and children over 12 years - use only as directed. - do not use on children under 12 years of age. - use up to 8 hours, repeat once if necessary. - reseal pouch containing unused patches.

STORAGE AND HANDLING SECTION

STORAGE AND HANDLING SECTION

Storage: Store in a cool and dry location out of direct sunlight.

OTC - QUESTIONS SECTION

OTC - QUESTIONS SECTION

Questions: Phone: 608-362-6915 E-mail: drohpatch@gmail.com

DOSAGE & ADMINISTRATION SECTION

DOSAGE & ADMINISTRATION SECTION

Dosage and administration: Use up to 8 hours, repeat once if necessary.

Source Document#

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