FDA.reportPublic FDA data

BLUESPRING Doctor's Pain Formula Pain Relief Cream

Manufacturer
ACA MANAGEMENT LLC | Pure Source, LLC
Effective date
2025-07-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:07:26

Label at a glance#

ProductBLUESPRING Doctors Pain Formula Pain Relief
Active ingredientMENTHOL
Label structure8 sections

Indications and uses

For the temporary relief of minor aches and pains associated with • arthritis • simple backache • sprains • strains • bruises

Dosage and administration

Apply to affected area not more than 3 or 4 times a day. Consult a doctor before using for children under 12 for arthritic conditions and for all children under 2 years of age for all other uses.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol, USP 1.4%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains associated with • arthritis • simple backache • sprains • strains • bruises

Warnings:

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

on wounded, damaged or irritated skin.

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes or mucous membranes. 
  • Do not bandage tightly

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • you experience a rash and/or a reaction
  • condition worsens or if symptoms persist for more than 10 days or clear up and occur again within few days.

If Pregnant or Breast-Feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use. Consult a doctorbefore use on children under 12 years of age if arthritis conditions are present. For all other listed uses, consult a doctor before use on children under 2 years of age.

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.

Other information

SPL UNCLASSIFIED SECTION

Store at room temperature.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply to affected area not more than 3 or 4 times a day. Consult a doctorbefore using for children under 12 for arthritic conditions and for all children under 2 years of age for all other uses.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Anthemis Nobilis (Roman Chamomile) Oil, Aqua (Deionized Water), Argania Spinosa (Argan) Oil, Arnica Montana Flower Extract, Ascorbyl Palmitate (Vitamin C), Calendula Officinalis Extract, Caprylyl Glycol, Centaurea Cyanus (Cornflower) Extract, Chamomilla Recutita (Chamomile) Extract, Coriandrum Sativum (Coriander) Oil, Emu Oil, Glycerin (plant based), Hamamelis Virginiana (Witch Hazel), Lamium Album (White Nettle) Extract, Methylsulfonylmethane (MSM), Phenoxyethanol, Salix Nigra (Willow) Bark Extract, Sodium Cocoyl Isethionate, Sodium Hydroxide, Sorbitol, Tanacetum Parthenium (Feverfew) Extract, Tetrasodium EDTA, Tilia Cordata (Linden) Extract, Tocopheryl Acetate (Vitamin E), Vitis Vinifera (Grape) Seed Extract.

Questions or Comments?

OTC - QUESTIONS SECTION

Call 1-855-290-7111or visit www.painrelief.md

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label0Label0

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2391332menthol 1.4 % Topical CreamPSN1
2391332menthol 14 MG/ML Topical CreamSCD1
2391332menthol 1.4 % Topical CreamSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83591-629-00BLUESPRING Doctors Pain Formula Pain Relief355 mL in 1 JARCREAM3551

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83591-62983591-629-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
ARGAN OIL4V59G5UW9XIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
ASCORBYL PALMITATEQN83US2B0NIACT
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT
CAPRYLYL GLYCOL00YIU5438UIACT
CHAMOMILEFGL3685T2XIACT
CORIANDER1OV56052IKIACT
EMU OIL344821WD61IACT
GLYCERINPDC6A3C0OXIACT
WITCH HAZEL101I4J0U34IACT
DIMETHYL SULFONE9H4PO4Z4FTIACT
PHENOXYETHANOLHIE492ZZ3TIACT
SALIX NIGRA BARKQU52J3A5B3IACT
SODIUM COCOYL ISETHIONATE518XTE8493IACT
SODIUM HYDROXIDE55X04QC32IIACT
SORBITOL506T60A25RIACT
FEVERFEWZ64FK7P217IACT
EDETATE SODIUMMP1J8420LUIACT
TILIA CORDATA WHOLEW5E5UB44GDIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
VITIS VINIFERA SEEDC34U15ICXAIACT
MENTHOLL7T10EIP3AACTIB

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
BLUESPRING Doctors Pain Formula Pain ReliefMENTHOLACA MANAGEMENT LLC98f3f719-792f-4a93-95b1-90072e0f8bf42025-07-14WarningsExact identifier
ndc (package): 83591-629-00
ndc (product): 83591-629
ndc11 (package): 83591062900
spl id: 39e0ad70-7af0-cd09-e063-6394a90a0f22
spl set id: 98f3f719-792f-4a93-95b1-90072e0f8bf4

Reported adverse events (FAERS/openFDA)#

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