T-RELIEF LIDOCAINE HCL 4%- lidocaine hcl 4% cream

T-Relief Lidocaine HCL 4% by

Drug Labeling and Warnings

T-Relief Lidocaine HCL 4% by is a Otc medication manufactured, distributed, or labeled by Medinatura New Mexico Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients: Purpose
Lidocaine HCl 4% .........................Topical Anesthetic

ASK DOCTOR

Stop use and ask a doctor:
If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor.

DO NOT USE

Do not use:
In large quantities, particularly over raw surfaces or blistered areas.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.
If swallowed, get medical help or contact a Poison
Control Center right away.

PREGNANCY OR BREAST FEEDING

If pregnant or breast-feeding, ask a health
professional before use.

PURPOSE

Uses
For the temporary relief of pain. Also relieves itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites, minor
skin irritations and rashes due to poison ivy.

QUESTIONS

Questions?

Call Weekdays 10am-6pm Eastern 1.844.MediNatura (1-844-633-4628) or email info@MediNatura.com

WHEN USING

When using this product:
Use only as directed.
Avoid contact with eyes.

WARNINGS

For external use only

DOSAGE & ADMINISTRATION

Directions:
Twist off cap and remove foil seal.
Adults and children 4 years of age and
older: Apply to affected area not more than 3 to
4 times daily.
Children under 4 years of age: do not use,
consult a doctor.

INACTIVE INGREDIENT

Inactive ingredients
Organic Aloe vera oil (Organic Aloe vera powder,
Organic Soybean oil, Vitamin E), Arnica,
Calendula, Caprylic/Capric triglyceride, Carbopol
Ultrez 10, Carrageenan, Chamomille, Organic
Coconut oil, Echinacea, Hypericum, Millefolium,
Phenoxyethanol, Purified water, Organic Safflowe
oil, Organic Shea butter, Sodium hydroxide, Sodium
polyacrylate, Sunflower seed wax

INDICATIONS & USAGE

• For the temporary relief of pain.
• Also relieves itching associated with minor burns, sunburn, minor cuts, scrapes, inspect bites, minor skin irritations and rashes due to poison ivy.

INDICATIONS & USAGE

• For the temporary relief of pain.
• Also relieves itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites, minor skin irritations and rashes due to poison ivy.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

T-RELIEF LIDOCAINE HCL 4% 
lidocaine hcl 4% cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62795-6050
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	3.4 g  in 85 g

Inactive Ingredients
Ingredient Name	Strength
SAFFLOWER OIL (UNII: 65UEH262IS)	0.17 g  in 85 g
CHONDRUS CRISPUS (UNII: OQS23HUA1X)	0.0026 g  in 85 g
HYPERICUM PERFORATUM WHOLE (UNII: XK4IUX8MNB)	0.000102 g  in 85 g
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.0000023 g  in 85 g
SOYBEAN OIL (UNII: 241ATL177A)	0.0002 g  in 85 g
MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ)	0.077 g  in 85 g
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)	0.00086 g  in 85 g
ARNICA MONTANA (UNII: O80TY208ZW)	0.0036 g  in 85 g
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)	0.425 g  in 85 g
PHENOXYETHANOL (UNII: HIE492ZZ3T)	0.425 g  in 85 g
ACHILLEA MILLEFOLIUM WHOLE (UNII: 2FXJ6SW4PK)	0.23 g  in 85 g
TOCOPHEROL (UNII: R0ZB2556P8)	0.0000001 g  in 85 g
SHEA BUTTER (UNII: K49155WL9Y)	4.25 g  in 85 g
POLYACRYLIC ACID (800000 MW) (UNII: D0I6NSZ87U)	0.51 g  in 85 g
COCONUT OIL (UNII: Q9L0O73W7L)	4.25 g  in 85 g
WATER (UNII: 059QF0KO0R)	67.4 g  in 85 g
SODIUM HYDROXIDE (UNII: 55X04QC32I)	0.128 g  in 85 g
HELIANTHUS ANNUUS (SUNFLOWER) SEED WAX (UNII: 42DG15CHXV)	0.25 g  in 85 g
ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX)	0.638 g  in 85 g

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62795-6050-7	85 g in 1 TUBE; Type 0: Not a Combination Product	11/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	11/01/2025

Labeler - Medinatura New Mexico Inc. (079324099)

Registrant - Medinatura New Mexico Inc. (079324099)