Rite Aid Hot and Cold Roll On

Manufacturer: Rite Aid | Derma Care Research Labs, LLC
Effective date: 2024-12-15
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 00:43:48

Label at a glance#

ProductRite Aid Hot and Cold Roll On

Active ingredientMENTHOL

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol 16%

OTC - PURPOSE SECTION

External Analgesic

INDICATIONS & USAGE SECTION

For the temporary relief of minor pain associated with arthritis, simple backache, muscle strains, sprains, bruises, and cramps.

WARNINGS SECTION

Flammable--keep away from fire or flame.

For external use only.

When using this product keep out of eyes, do not apply to wounds or damaged skin, do not bandage tightly.

Stop use and ask a doctor if condition worsens, symptoms last more than 7 days or clear and occur again within a few days, and redness or irritation develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If product is swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Clean affected area before applying product • adults and children 12 years and older, apply to affected area not more
than 3 to 4 times daily. • Children under 12 years old, ask a doctor

INACTIVE INGREDIENT SECTION

Acrylates/C10-30 alkyl acrylate crosspolymer, alcohol denat., glycerin, phenoxyethanol, propylene glycol, water, xanthan gum

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
866084	menthol 16 % Topical Solution	PSN	2
866084	menthol 160 MG/ML Topical Solution	SCD	2
866084	menthol 16 % Topical Solution	SY	2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
11822-1015-1	Rite Aid Hot and Cold Roll On	71 g in 1 BOTTLE, PLASTIC	LIQUID	71		2
11822-1015-1	Rite Aid Hot and Cold Roll On	1 in 1 CARTON	LIQUID	1		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11822-1015	RITE AID HOT AND COLD ROLL ON (MENTHOL 16%) LIQUID [RITE AID]	2	Current NDC, 2 package rows	20241217_fc4b2635-280b-267f-e053-6294a90a5e22.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

Rite Aid Hot and Cold Roll On
Menthol 16%
PHENOXYETHANOL
MENTHOL
CARBOMER INTERPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)
GLYCERIN
WATER
ALCOHOL
PROPYLENE GLYCOL
XANTHAN GUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
11822-1015	11822-1015-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
PHENOXYETHANOL	HIE492ZZ3T	IACT
MENTHOL	L7T10EIP3A	ACTIB
CARBOMER INTERPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)	132584PQMO	IACT
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
XANTHAN GUM	TTV12P4NEE	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Rite Aid Hot and Cold Roll On	MENTHOL 16%	Rite Aid	fc4b2635-280b-267f-e053-6294a90a5e22	2024-12-15	Warnings	Exact identifier ndc (package): 11822-1015-1 ndc (product): 11822-1015 ndc11 (package): 11822101501 spl id: 2956a130-bb14-2b35-e063-6394a90a9017 spl set id: fc4b2635-280b-267f-e053-6294a90a5e22

Reported adverse events (FAERS/openFDA)#

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