Rite Aid Hot & Cold Pain Relief Cream

Manufacturer: Rite Aid | ANICARE PHARMACEUTICALS PRIVATE LIMITED
Effective date: 2024-12-18
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 00:45:04

Label at a glance#

ProductRite Aid Hot and Cold Pain Relief Pain Relieving

Active ingredientLIDOCAINE, MENTHOL

Label structure8 sections

Indications and uses

Temporarily relieves minor pain

Dosage and administration

adults and children over 12 years: apply a thin layer to affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period children 12 years or younger: ask a doctor

Contacts and useful links#

PhonePoison Help1-800-222-1222

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Rite Aid Lidocaine-Menthol Pain Relief Cream

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine HCl 4%

Menthol 1%

Purposes

OTC - PURPOSE SECTION

Topical anesthetic

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves minor pain

Warnings

WARNINGS SECTION

For external use only

Avoid contact with eyes

Do not use

OTC - DO NOT USE SECTION

on large areas of the body or on cut, irritated or swollen skin
on puncture wounds
for more than one week without consulting a doctor

When using this product

OTC - WHEN USING SECTION

Use only as directed. Read and follow all directions and warnings on this carton.
do not allow contact with eyes

do not bandage or apply local heat (such as heating pads) to the area of use

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children and pets.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

adults and children over 12 years:

apply a thin layer to affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period

children 12 years or younger: ask a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe vera leaf, carbopol 940, cetostearyl alcohol, dimethicone 350, edetate disodium, glycerin, glyceryl monostearate, isopropyl alcohol, phenoxyethanol, polysorbate 60, steareth 2, steareth 21, water

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
250912	lidocaine 4 % / menthol 1 % Topical Cream	PSN	2
250912	lidocaine 40 MG/ML / menthol 10 MG/ML Topical Cream	SCD	2
250912	lidocaine 4 % / menthol 1 % Topical Cream	SY	2

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
LIDOCAINE Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
11822-4216-1	2025-07-29	C162847	48780-1	3b156c62-313f-fb37-e063-e6dba90a4e07	Rite Aid Hot & Cold Pain Relief Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
11822-4216-1	Rite Aid Hot and Cold Pain ReliefPain Relieving	1 in 1 CARTON	CREAM	1		2
11822-4216-1	Rite Aid Hot and Cold Pain ReliefPain Relieving	76.5 g in 1 TUBE	CREAM	76.5		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11822-4216	RITE AID HOT AND COLD PAIN RELIEF PAIN RELIEVING (LIDOCAINE HCL AND MENTHOL) CREAM [RITE AID]	2	Legacy NDC, 2 package rows	20241220_e08e7c5b-34ba-da8a-e053-2a95a90af497.zip

Products#

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

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

Rite Aid Hot and Cold Pain Relief Pain Relieving
Lidocaine HCl and Menthol
ALOE VERA LEAF
CARBOMER 940
DIMETHICONE 350
CETOSTEARYL ALCOHOL
GLYCERIN
ISOPROPYL ALCOHOL
PHENOXYETHANOL
EDETATE DISODIUM
STEARETH-2
GLYCERYL MONOSTEARATE
POLYSORBATE 60
STEARETH-21
WATER
LIDOCAINE
MENTHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
11822-4216	11822-4216-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALOE VERA LEAF	ZY81Z83H0X	IACT
CARBOMER 940	4Q93RCW27E	IACT
DIMETHICONE 350	2Y53S6ATLU	IACT
CETOSTEARYL ALCOHOL	2DMT128M1S	IACT
GLYCERIN	PDC6A3C0OX	IACT
ISOPROPYL ALCOHOL	ND2M416302	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
EDETATE DISODIUM	7FLD91C86K	IACT
STEARETH-2	V56DFE46J5	IACT
GLYCERYL MONOSTEARATE	230OU9XXE4	IACT
POLYSORBATE 60	CAL22UVI4M	IACT
STEARETH-21	53J3F32P58	IACT
WATER	059QF0KO0R	IACT
LIDOCAINE	98PI200987	ACTIB
MENTHOL	L7T10EIP3A	ACTIB

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
29915354-4675-7444-e063-6294a90a0fd1			e08e7c5b-34ba-da8a-e053-2a95a90af497	2024-12-18	Warnings	Exact identifier spl id: 29915354-4675-7444-e063-6294a90a0fd1 spl set id: e08e7c5b-34ba-da8a-e053-2a95a90af497

Reported adverse events (FAERS/openFDA)#

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