DB Pain Relieving Cream

Manufacturer
United Laboratories Manufacturing, LLC
Effective date
2022-11-15
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 21:47:19

Label at a glance#

ProductDB Pain Relieving
Active ingredientPSEUDOGNAPHALIUM OBTUSIFOLIUM, APIS MELLIFERA, GELSEMIUM SEMPERVIRENS ROOT
Label structure6 sections

Dosage and administration

Generously apply and massage into all surfaces of the feet, heels, and toes twice daily. Apply to legs as needed. Most beneficial when appied after bathing, showering, or a foot soak. There is no scientifica evidence that this product works. The product's claims are based on theories of homeophathy from the 1700s tht are not accepted by most medical experts.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Gnaphalium polycephalum
Honeybee (Apis Mellifica)
Yellow Jessamine (Gelsemium sempervirens)

Purpose

OTC - PURPOSE SECTION

Relieves Foot Pain

External Analgesic

Use

INDICATIONS & USAGE SECTION

Temporarily relieves leg and foot pain.

Warnings

WARNINGS SECTION

For external use only.

Avoid contact with eyes.

Do not use

OTC - DO NOT USE SECTION

  • On open wounds
  • Cuts
  • Damaged skin
  • Infected skin.

Stop Use and Ask a Doctor

OTC - STOP USE SECTION

If symptoms persist for more than 7 days or worsen.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Generously apply and massage into all surfaces of the feet, heels, and toes twice daily.

Apply to legs as needed.

Most beneficial when appied after bathing, showering, or a foot soak.

There is no scientifica evidence that this product works.

The product's claims are based on theories of homeophathy from the 1700s tht are not accepted by most medical experts.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, canola oil, beeswax, octyl stearate, wintergreen oil, tocopheryl acetate, triethanolamine, oil of bergamot, camphor, menthol, eucalyptus oil, steareth-10, steareth-21, ceteth-20, stearic acid, cetyl alcohol, glyceryl stearate, peg-100, propylene glycol, xanthan gum, methylparaben, propylparaben, carbomer 940, imidazolidinyl urea.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

United labs green 1United labs green 1United labs green 2United labs green 2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62400-0026DB PAIN RELIEVING (PSEUDOGNAPHALIUM OBTUSIFOLIUM,APIS MELLIFERA,GELSEMIUM SEMPERVIRES ROOT) CREAM [UNITED LABORATORIES MANUFACTURING, LLC]5Legacy NDC20221122_50de9545-93ce-4bcc-86c8-72f49e61ae2c.zip

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62400-002662400-0026-1, 62400-0026-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 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
3f0144eb-621e-cea5-e063-6294a90ac65d50de9545-93ce-4bcc-86c8-72f49e61ae2c2025-09-17WarningsExact identifier
spl set id: 50de9545-93ce-4bcc-86c8-72f49e61ae2c

Reported adverse events (FAERS/openFDA)#

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