FDA.reportPublic FDA data

Inmotion Pain Creme Ultra Strength

Manufacturer
Inmotion Products LLC
Effective date
2019-05-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:59:29

Label at a glance#

ProductInmotion Pain Creme Ultra Strength
Active ingredientMenthol, Unspecified Form, Trolamine Salicylate
Label structure9 sections

Indications and uses

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

Dosage and administration

adults and children over 12 years apply generously to affected area massage painful area until thoroughly absorbed into skin repeat as necessary up to 3 times daily

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol 4%, Trolamine Salicylate 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:

  • arthritis
  • simple backache
  • muscle strains
  • sprains
  • bruises
  • cramps

Warnings

WARNINGS SECTION

For external use only

Use only as directed

When to use this product

SPL UNCLASSIFIED SECTION

  • do not bandage tightly or use with a heating pad
  • avoid contact with eyes and mucous membranes
  • do not apply to wounds or damaged, broken or irritated skin
  • if a burning sensation occurs, discontinue use immediately
  • do not expose the area treated with product to heat or direct sunlight

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • redness is present
  • irritation develops
  • symptoms persist for more than 7 days or clear up and occur again within a few days.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding: ask a health professional

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

  • adults and children over 12 years
  • apply generously to affected area
  • massage painful area until thoroughly absorbed into skin
  • repeat as necessary up to 3 times daily

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Sesame Oil, Cetylated Fatty Acids (Cetyl Myristyloleate), Glycerin, Organic Hempseed, B-Caryophilene 8%, Boswellia serrata, Lavender Oil, PEG 100 Stearate, Glyceryl Monolaurate, Cetearyl Alchohol, Cetearyl Glucoside, Cyclopentasiloxane, Cetyl Alchohol, Phosphatidylcholine, Glyceryl Stearate, Butyrospermum Parkii (SheaButter), Aloe Barbadensis Leaf Juice, Dimethicone, Ethyl Alchohol, SclerotiumGum, PotassiumSorbate, Ascorbyl Palmitate, Vitamin E Acetate, Ethyl Lauoryl Arginate, Polyaminopropyl Biguanide

SPL UNCLASSIFIED SECTION

Distributed By:
InMotion Products LLC
4639 Torrey Circle,
M-102, San Diego, Ca 92130

PRINCIPAL DISPLAY PANEL - 2.5 oz Tube Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ULTRA STRENGTH

LIPOSOME FORMULA
FOR FAST ABSORPTION

INMOTION
PAIN CREME

FAST ACTING PAIN RELIEF

Arthritis | Back Pain | Knee Pain
Foot Pain | Elbow Pain

Featuring
ORGANIC HEMPSEED OIL

B-Caryophllene, Organic Hempseed, Boswellia, Cetyl Myristoleate

INMOTION
ESSENTIALS
FORMULA

Non-Staining
No Strong Odor
4% Menthol

NET WT. 2.5 oz.

PRINCIPAL DISPLAY PANEL - 2.5 oz Tube Carton
PRINCIPAL DISPLAY PANEL - 2.5 oz Tube Carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72581-428-732021-01-29C16284748780-1ba0f9c33-591c-a910-e053-dadaa90a0b85Inmotion Pain Creme Ultra Strength

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72581-428-73Inmotion Pain Creme Ultra Strength73 mL in 1 TUBECREAM731
72581-428-73Inmotion Pain Creme Ultra Strength1 in 1 CARTONCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72581-428INMOTION PAIN CREME ULTRA STRENGTH (MENTHOL, UNSPECIFIED FORM AND TROLAMINE SALICYLATE) CREAM [INMOTION PRODUCTS LLC]1Legacy NDC, 2 package rows20190516_779d027c-c975-4aeb-b976-e23955bd3b5f.zip

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72581-42872581-428-73

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 matching rows.

Name, UNII, Kind table
NameUNIIKind
Menthol, Unspecified FormL7T10EIP3AACTIB
Trolamine SalicylateH8O4040BHDACTIB
Water059QF0KO0RIACT
Sesame OilQX10HYY4QVIACT
Cetyl Myristoleate87P8K33Q5XIACT
GlycerinPDC6A3C0OXIACT
Indian Frankincense4PW41QCO2MIACT
Lavender OilZBP1YXW0H8IACT
Peg-100 StearateYD01N1999RIACT
Glyceryl LaurateY98611C087IACT
Cetostearyl Alcohol2DMT128M1SIACT
Cetearyl Glucoside09FUA47KNAIACT
Cyclomethicone 50THT5PCI0RIACT
Cetyl Alcohol936JST6JCNIACT
Glyceryl Monostearate230OU9XXE4IACT
Shea ButterK49155WL9YIACT
Aloe Vera LeafZY81Z83H0XIACT
Dimethicone92RU3N3Y1OIACT
Alcohol3K9958V90MIACT
Betasizofiran2X51AD1X3TIACT
Potassium Sorbate1VPU26JZZ4IACT
Ascorbyl PalmitateQN83US2B0NIACT
.Alpha.-Tocopherol Acetate9E8X80D2L0IACT
Ethyl Lauroyl ArginateE0K8J7A41BIACT

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
129f6a1a-480b-40ab-aacf-11cc8f550f3f779d027c-c975-4aeb-b976-e23955bd3b5f2019-05-15WarningsExact identifier
spl id: 129f6a1a-480b-40ab-aacf-11cc8f550f3f
spl set id: 779d027c-c975-4aeb-b976-e23955bd3b5f

Reported adverse events (FAERS/openFDA)#

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