STEEL CITY GREATS MENTHOL REVIVE MENTHOL PAIN CREAM

Manufacturer
RENU LABORATORIES, INC.
Effective date
2023-09-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:24:13

Label at a glance#

ProductSTEEL CITY GREATS MENTHOL REVIVE
Active ingredientMENTHOL
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol 5%

OTC - PURPOSE SECTION

Topical Analgesic

INDICATIONS & USAGE SECTION

For temporary relief of minor aches and pains associated with

  • arthritis
  • simple backache
  • muscle strains
  • sprains
  • bruises

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

Do not bandage tightly

  • avoid contact with eyes
  • do not apply to wounds or damaged skin
  • do not use with heating pads or other heating devices.

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

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

DOSAGE & ADMINISTRATION SECTION

Instructions: Massage into skin until thoroughtly absorbed. Repeat as needed. Store at room temperature.

INACTIVE INGREDIENT SECTION

Butyrospermum Parkii (Shea) Butter, Cannabis Sativa (Hemp) Seed Oil, with a proprietary blend of terpenes (alpha-bisabolol,

alpha-humulene, beta-caryophyllene, caryophyllene oxide, gualol, linalool),

Cetearyl Alcohol, Cetearyl Glucoside, Cocos Nucifera (Coconut) Oil, C13-14 Isoparaffin, Deionized Water, Emulsifying Wax, Ethylhexylglycerin, Fragrance, Hemp-derived Cannabichromene (CBC), Cannabidiol (CBD), and Cannabigerol (CBG),

Glyceryl Stearate, Hamamelis Virginiana (Witch Hazel), Laureth-7, Magnesium Sulfate, Mangifera Indica (Mango) Seed Buter,

Mentha Piperita (Peppermint) Oil, Olea Europaea (Olive) Oil, Olus Oil (Vegetable), PEG-100 Stearate, Phenoxyethanol, Polyacrylamide, Stearic Acid

RECENT MAJOR CHANGES SECTION

Indications and Usage This is a clone of another product. Only slight changes to wording have happened. Nothing major.

Dosage and Administration - Directions were simplified.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

JAR LABEL FOR PRODUCT

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Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76348-99876348-998-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

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
19b2eeec-8f62-4956-e063-6394a90aeda106820449-1fe0-0e7d-e063-6294a90aad522024-05-30WarningsExact identifier
spl set id: 06820449-1fe0-0e7d-e063-6294a90aad52

Reported adverse events (FAERS/openFDA)#

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