FDA.reportPublic FDA data

Dr. Ds Super 7 Pain Relief

Manufacturer
Promedx Innovations Inc
Effective date
2021-01-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:54:31

Label at a glance#

ProductDr. Ds Super 7 Pain Relief
Active ingredientMENTHOL, MENTHYL SALICYLATE, (+/-)-
Label structure8 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints associated with simple backache arthritis strains and sprains bruises

Dosage and administration

Adults and children 2 years of age and older: shake bottle before use apply a thin and even coat to affected area not more than 3 to 4 times daily rub and/or massage into skin until the preparation disappears Children (2 to 12 years old) ask a doctor application should be supervised by an adult

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthyl Salicylate 10%

Menthol 2%

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints associated with

  • simple backache
  • arthritis
  • strains and sprains
  • bruises

Warnings

WARNINGS SECTION

For external use only

Allergy alert

WARNINGS SECTION

  • do not use if you are allergic to plants of the Asteraceae / Compositae / Daisy family

When using this product

OTC - WHEN USING SECTION

  • avoid contact with the eyes and mucous membranes
  • do not apply to wounds or damaged skin
  • do not bandage tightly
  • do not apply with external heat, such as an electric pad, as this may result in excessive skin irritation or skin burn

Ask a healthcare professional before use if you are

OTC - ASK DOCTOR/PHARMACIST SECTION

  • taking anticoagulant medications

Stop using and ask a healthcare professional if

OTC - STOP USE SECTION

  • condition worsens
  • symptoms last more than 7 days or clear up and occur again within a few days
  • if a rash develops, or you become hypersensitive and/or burning, blistering or swelling occurs, discontinue use and seek medical help immediately

If pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

  • ask a healthcare professional before use

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 2 years of age and older:

  • shake bottle before use
  • apply a thin and even coat to affected area not more than 3 to 4 times daily
  • rub and/or massage into skin until the preparation disappears

Children (2 to 12 years old)

  • ask a doctor
  • application should be supervised by an adult

Other information

OTHER SAFETY INFORMATION

  • store at room temperature 15°C - 30°C (59°F - 86°F)
  • do not use if quality seal is missing or broken
  • store in airtight, light-resistant container

Inactive ingredients

INACTIVE INGREDIENT SECTION

Arnica Montana Flower Extract, Benzoic Acid, Brassica Campestris (Rapeseed) Seed Oil, Citric Acid, Dehydroacetic Acid, Eucalyptus Globulus Leaf Essential Oil, Glycerin, Linum Usitatissimum (Linseed) Seed Extract, MSM, Myristyl Myristate, Neopentyl Glycol Dicaprylate/Dicaprate, Peppermint Oil (Mentha piperita), Phenoxyethanol, Rosmarinus Officinalis (Rosemary) Leaf Extract, Silica, Sodium Stearoyl Glutamate, Water, Xanthan Gum

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DR. D'S

SUPER 7

Enhanced Topical Pain Relief

NEW

For relief of:

Muscle, Joint

and Arthritic Pain

TRIPLE CARRIER SYSTEM

  • Doctor Developed
  • 7 Powerful Natural Ingredients
  • Easy to Use Applicator
  • Paraben and PEG Free

88 mL

NDC 72246-112-01

ProMedx-Dr.-D's-Super-7-US-88-ml-01ProMedx-Dr.-D's-Super-7-US-88-ml-01

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72246-112-012025-01-30C16284748780-12cef2736-6ecc-d83d-e063-dadaa90ab31faaca1fbf-aed6-4fe0-9821-6fa897b5d41e

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72246-112DR. DS SUPER 7 PAIN RELIEF (MENTHYL SALICYLATE AND MENTHOL) CREAM [PROMEDX INNOVATIONS INC]2Legacy NDC20210129_aaca1fbf-aed6-4fe0-9821-6fa897b5d41e.zip

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72246-11272246-112-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZOIC ACID8SKN0B0MIMIACT
DEHYDROACETIC ACID2KAG279R6RIACT
EUCALYPTUS OIL2R04ONI662IACT
PEPPERMINT OILAV092KU4JHIACT
NEOPENTYL GLYCOL DICAPRYLATE/DICAPRATEVLW429K27KIACT
MYRISTYL MYRISTATE4042ZC00DYIACT
BRASSICA RAPA SUBSP. OLEIFERA OILN4G8379626IACT
SILICON DIOXIDEETJ7Z6XBU4IACT
ROSEMARYIJ67X351P9IACT
XANTHAN GUMTTV12P4NEEIACT
GLYCERINPDC6A3C0OXIACT
SODIUM STEAROYL GLUTAMATE65A9F4P024IACT
DIMETHYL SULFONE9H4PO4Z4FTIACT
WATER059QF0KO0RIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
FLAX SEED4110YT348CIACT
PHENOXYETHANOLHIE492ZZ3TIACT
MENTHOLL7T10EIP3AACTIB
MENTHYL SALICYLATE, (+/-)-43XOA705ZDACTIM

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
b9e9ab5b-aff7-e8cf-e053-2995a90a93f5aaca1fbf-aed6-4fe0-9821-6fa897b5d41e2021-01-27WarningsExact identifier
spl id: b9e9ab5b-aff7-e8cf-e053-2995a90a93f5
spl set id: aaca1fbf-aed6-4fe0-9821-6fa897b5d41e

Reported adverse events (FAERS/openFDA)#

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