FDA.reportPublic FDA data

Rite Aid Ultra Strength Muscle Rub

Manufacturer
Rite Aid Corporation | Anicare Pharmaceuticals Pvt. Ltd.
Effective date
2024-12-18
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:45:07

Label at a glance#

ProductRite Aid Ultra Strength Muscle Rub
Active ingredientMENTHOL, UNSPECIFIED FORM, CAMPHOR (SYNTHETIC), METHYL SALICYLATE
Label structure14 sections

Dosage and administration

temporarily relieves the minor aches and pains of muscles and joints associated with: simple backache arthritis strains bruises sprains

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Camphor 4%

Menthol 10%

Methyl salicylate 30%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Topical Analgesic

Topical Analgesic

Directions

INDICATIONS & USAGE SECTION

temporarily relieves the minor aches and pains of muscles and joints associated with:

  • simple backache
  • arthritis
  • strains
  • bruises
  • sprains

Warnings

WARNINGS SECTION

For external use only.

Do not Use

OTC - DO NOT USE SECTION

  • on wounds or damaged skin
  • with a heating pad
  • on a child under 12 years of age with arthritis-like conditions

Ask Doctor

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have redness over affected area

When Using Section

OTC - WHEN USING SECTION

  • use only as directed
  • avoid contact with eyes or mucous membranes
  • do not bandage tightly

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • symptoms last more than 7 days or clear up and occur again within a few days

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily
  • children under 12 years of age: consult a physician

Other Information

OTHER SAFETY INFORMATION

  • store at 20° to 25°C (68° to 77°F)
  • do not use if tube seal under cap is broken

Inactive Ingredients

INACTIVE INGREDIENT SECTION

carbomer homopolymer type C, cetostearyl alcohol, cetyl alcohol, glycerine monostearate, peg-100 stearate, Phenoxyethanol, polysorbate 60, sodium benzoate, stearic acid, trolamine, water

Rite Aid Ultra Strength Muscle Rub

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
283083camphor 4 % / menthol 10 % / methyl salicylate 30 % Topical CreamPSN3
283083camphor 40 MG/ML / menthol 100 MG/ML / methyl salicylate 300 MG/ML Topical CreamSCD3
283083camphor 4 % / menthol 10 % / methyl salicylate 30 % Topical CreamSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11822-9993-12025-07-29C16284748780-13b156c62-317a-fb37-e063-e6dba90a4e07Rite Aid Ultra Strength Muscle Rub

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11822-9993-1Rite Aid Ultra Strength Muscle Rub113 g in 1 TUBECREAM1133
11822-9993-1Rite Aid Ultra Strength Muscle Rub1 in 1 CARTONCREAM13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-9993RITE AID ULTRA STRENGTH MUSCLE RUB (METHYL SALICYLATE 30.0%, CAMPHOR 4.0%, MENTHOL 10.0%) CREAM [RITE AID CORPORATION]32 package rows20241220_efa57b5c-b43a-b3f6-e053-2995a90acce2.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11822-999311822-9993-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB
CAMPHOR (SYNTHETIC)5TJD82A1ETACTIB
METHYL SALICYLATELAV5U5022YACTIB
PHENOXYETHANOLHIE492ZZ3TIACT
STEARIC ACID4ELV7Z65APIACT
CETYL ALCOHOL936JST6JCNIACT
POLYSORBATE 60CAL22UVI4MIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
CARBOMER 9404Q93RCW27EIACT
WATER059QF0KO0RIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
POLYOXYL 100 STEARATEYD01N1999RIACT
TROLAMINE9O3K93S3TKIACT
SODIUM BENZOATEOJ245FE5EUIACT

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
2991928b-cae6-1104-e063-6394a90ab333efa57b5c-b43a-b3f6-e053-2995a90acce22024-12-18WarningsExact identifier
spl id: 2991928b-cae6-1104-e063-6394a90ab333
spl set id: efa57b5c-b43a-b3f6-e053-2995a90acce2

Reported adverse events (FAERS/openFDA)#

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