BLUESPRING DOCTORS PAIN FORMULA PAIN RELIEF- menthol cream

BLUESPRING Doctors Pain Formula Pain Relief by

Drug Labeling and Warnings

BLUESPRING Doctors Pain Formula Pain Relief by is a Otc medication manufactured, distributed, or labeled by ACA MANAGEMENT LLC, Pure Source, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Product Facts

Active Ingredient

Menthol, USP 1.4%

Purpose

Topical Analgesic

Uses

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

Warnings:

For external use only

Do not use

on wounded, damaged or irritated skin.

When using this product

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

Stop use and ask a doctor if

• 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

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.

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

Other information

Store at room temperature.

Directions

• 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

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?

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

Package Labeling:

INGREDIENTS AND APPEARANCE

BLUESPRING DOCTORS PAIN FORMULA PAIN RELIEF 
menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83591-629
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	14 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
ARGAN OIL (UNII: 4V59G5UW9X)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
ASCORBYL PALMITATE (UNII: QN83US2B0N)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CHAMOMILE (UNII: FGL3685T2X)
CORIANDER (UNII: 1OV56052IK)
EMU OIL (UNII: 344821WD61)
GLYCERIN (UNII: PDC6A3C0OX)
WITCH HAZEL (UNII: 101I4J0U34)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SALIX NIGRA BARK (UNII: QU52J3A5B3)
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SORBITOL (UNII: 506T60A25R)
FEVERFEW (UNII: Z64FK7P217)
EDETATE SODIUM (UNII: MP1J8420LU)
TILIA CORDATA WHOLE (UNII: W5E5UB44GD)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
VITIS VINIFERA SEED (UNII: C34U15ICXA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83591-629-00	355 mL in 1 JAR; Type 0: Not a Combination Product	07/07/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	07/07/2025

Labeler - ACA MANAGEMENT LLC (119034214)

Registrant - Pure Source, LLC (080354456)