FDA.reportPublic FDA data

Topical Analgesic Lotion - Real Time Pain Relief Inc | Eisinger Smith LLC

Manufacturer
Real Time Pain Relief Inc | Eisinger Smith LLC
Effective date
2026-07-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-07-29 05:10:12

Label at a glance#

ProductOriginal Pain Relief
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure10 sections

Label contents#

Full prescribing information#

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Alcohol, Aloe Barbadensis Leaf Juice, Anthemis nobilis (Roman Chamomile), Arnica Montana Flower Extract, Butylene Glycol, C13-14 Isoparaffin, Calendula officinalis (Marigold), Caprylyl Glycol, Capsicum Frutescens Fruit, Centaurea cyanus (Cornflower), Chamomilla recutita (Matricaria chamomilla), Coriandrum Sativum (Coriander) Fruit Oil, Emu Oil, Fragrance, Glucosamine HCl, Hamamelis Virginian (Witch Hazel) Bark/Leaf/Twig Extract, Hypericum perforaturn (St. John’s Wort), Laureth-7, Methylsulfonylmethane, Phenoxyethanol, Polyacrylamide, Purified Water, Salix alba (Willow) Bark Extract, Sodium Chondroitin Sulfate, Sorbitol, Tilia cordata (Lime Tree).

OTC - ASK DOCTOR/PHARMACIST SECTION

Stop using and ask doctor if: Condition worsens. Symptoms persist for more than 7 days or clear up and occur again within a few days. Redness is present. Irritation develops.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If Pregnant or Breast-Feeding: ask a health professional before use. Keep all medicines out of reach of children. If swallowed get medical help or contact Poison Control Center right away.

WARNINGS SECTION

Warnings: For external use only

When using this product: Use only as directed. Avoid contact with eyes or mucous membranes. Do not apply to wounds or damaged skin. Do not bandage tightly.

DOSAGE & ADMINISTRATION SECTION

Menthol 1.25%

INDICATIONS & USAGE SECTION

Uses: Temporarily relieves minor pain associated with: Arthritis * Simple Backache *Muscle Strains *Sprains *Bruises *Cramps

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

OTC - PURPOSE SECTION

Topical Analgesic

OTC - QUESTIONS SECTION

877-787-7180

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Original Lotion 84573-100-06Original Lotion 84573-100-06Original Lotion 84573-100-01Original Lotion 84573-100-01Original Lotion 84573-100-02Original Lotion 84573-100-02Original Lotion 84573-100-03Original Lotion 84573-100-03Original Lotion 84573-100-04Original Lotion 84573-100-04Original Lotion 84573-100-05Original Lotion 84573-100-05Original Lotion 84573-100-06Original Lotion 84573-100-06

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130040232079078GTIN-13: 0040232079078
EAN-13: 0040232079078
GTIN-12: 040232079078
UPC-A: 040232079078
GTIN storage (14 digits): 00040232079078		Original_4oz_Label_2025.jpg
BarcodeEAN-130810042760462GTIN-13: 0810042760462
EAN-13: 0810042760462
GTIN-12: 810042760462
UPC-A: 810042760462
GTIN storage (14 digits): 00810042760462		Original_3oz_Label_2025 (1).jpg

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84573-10084573-100-01, 84573-100-02, 84573-100-03, 84573-100-04, 84573-100-05, 84573-100-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB
LAURETH-7Z95S6G8201IACT
PHENOXYETHANOLHIE492ZZ3TIACT
ALCOHOL3K9958V90MIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
CENTAUREA CYANUS FLOWERQZ239038YCIACT
HYPERICUM PERFORATUM LEAFDOC7OB843YIACT
DICHLORO(METHYLSULFONYL)METHANET9UT3SG9V4IACT
SORBITOL506T60A25RIACT
FRAGRANCE 135765EM498GW35IACT
SALIX ALBA BARK205MXS71H7IACT
WATER059QF0KO0RIACT
CAPSICUM OLEORESINUW86K581WYIACT
SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW)H5BJH23Z9AIACT
TILIA CORDATA FLOWERCFN6G1F6YKIACT
ARNICA MONTANAO80TY208ZWIACT
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT
HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF WATER8FP93ED6H2IACT
CORIANDER OIL7626GC95E5IACT
POLYACRYLAMIDE (10000 MW)E2KR9C9V2IIACT
GLUCOSAMINE HCL750W5330FYIACT
ALOE BARBADENSIS LEAFZY81Z83H0XIACT
ANTHEMIS NOBILIS FLOWER OILUB27587839IACT
C13-14 ISOPARAFFINE4F12ROE70IACT
CAPRYLYL GLYCOL00YIU5438UIACT
EMU OIL344821WD61IACT

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
Original Pain ReliefTOPICAL ANALGESIC LOTIONReal Time Pain Relief Inc579bd303-9a50-4d66-e063-6294a90a61412026-07-27WarningsExact identifier
ndc (package): 84573-100-01
ndc (package): 84573-100-04
ndc (package): 84573-100-05
ndc (package): 84573-100-06
ndc (package): 84573-100-03
ndc (package): 84573-100-02
ndc (product): 84573-100
ndc11 (package): 84573010006
ndc11 (package): 84573010002
ndc11 (package): 84573010001
ndc11 (package): 84573010005
ndc11 (package): 84573010004
ndc11 (package): 84573010003
spl id: 579bd303-9a51-4d66-e063-6294a90a6141
spl set id: 579bd303-9a50-4d66-e063-6294a90a6141

Reported adverse events (FAERS/openFDA)#

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