RITE AID ULTRA STRENGTH MUSCLE RUB- methyl salicylate 30.0%, camphor 4.0%, menthol 10.0% cream

Rite Aid Ultra Strength Muscle Rub by

Drug Labeling and Warnings

Rite Aid Ultra Strength Muscle Rub by is a Otc medication manufactured, distributed, or labeled by Rite Aid Corporation, Anicare Pharmaceuticals Pvt. Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Camphor 4%

Menthol 10%

Methyl salicylate 30%

SPL UNCLASSIFIED SECTION

Purpose

Topical Analgesic

Topical Analgesic

Topical Analgesic

Directions

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

• simple backache
• arthritis
• strains
• bruises
• sprains

Warnings

For external use only.

Do not Use

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

Ask Doctor

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

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

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

Keep out of reach of children

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

Directions

• 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

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

Inactive Ingredients

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

Questions

www.riteaid.com

Rite Aid Ultra Strength Muscle Rub

INGREDIENTS AND APPEARANCE

RITE AID ULTRA STRENGTH MUSCLE RUB 
methyl salicylate 30.0%, camphor 4.0%, menthol 10.0% cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11822-9993
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	100 mg  in 1 g
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	40 mg  in 1 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	300 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
PHENOXYETHANOL (UNII: HIE492ZZ3T)
STEARIC ACID (UNII: 4ELV7Z65AP)
CETYL ALCOHOL (UNII: 936JST6JCN)
POLYSORBATE 60 (UNII: CAL22UVI4M)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
CARBOMER 940 (UNII: 4Q93RCW27E)
WATER (UNII: 059QF0KO0R)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
POLYOXYL 100 STEARATE (UNII: YD01N1999R)
TROLAMINE (UNII: 9O3K93S3TK)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11822-9993-1	1 in 1 CARTON	03/01/2023
1		113 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	03/01/2023

Labeler - Rite Aid Corporation (014578892)

Establishment
Name	Address	ID/FEI	Business Operations
Anicare Pharmaceuticals Pvt. Ltd.		916837425	manufacture(11822-9993)