BIOFREEZE OVERNIGHT RELIEF- menthol, unspecified form patch 
RB Health (US) LLC

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Biofreeze ®Overnight Relief Patch

Drug Facts

Active ingredient

Menthol 5%

Purpose

Pain Relieving Patch

Uses

Temporarily relieves minor aches and pains of muscles and joints associated with:

Warnings

For external use only.

When using this product

  • use only as directed
  • avoid contact with the eyes or on mucous membranes
  • do not apply to wounds or damaged skin
  • do not apply to irritated skin or if excessive irritation develops
  • do not bandage tightly or use with heating pad or device

Stop use and ask a doctor if

  • you experience pain, swelling or blistering of the skin
  • condition worsens, or if symptons persist for more than 7 days or clear up and occur again within a few days
  • arthritic pain persists for more than 10 days, or redness is present

If pregnant or breast-feeding,ask a health professional before use.

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Inactive ingredients

Benzalkonium Chloride, Carboxymethylcellulose Sodium, Dihydroxyaluminum Aminoacetate, Edetate Disodium, Glycerin, Kaolin, Lauralkonium Chloride, Lavender Oil, Mineral Oil, Petrolatum, Polyacrylic Acid, Polysorbate 80, Povidone, Propylene Glycol, Purified Water, Sodium Polyacrylate, Tartaric Acid, Titanium Dioxide

Questions or comments?

1-866-682-4639

Dist. by: RB Health (US)
Parsippany, NJ 07054-0224

Made in China

PRINCIPAL DISPLAY PANEL - 4 Patch Pouch Carton

CLINICALLY
RECOMMENDED

NDC 59316-005-04

BIOFREEZE ®
COOL THE PAIN

OVERNIGHT
RELIEF
PATCHES

MENTHOL-TOPICAL
ANALGESIC

Overnight pain relief patch
Scented with lavender
essential oil

Designed to stay on
through the night

Optimal thickness is designed for comfort and flexibility

4 PATCHES

5.125 in x 2.6 in
(13 cm x 6.6 cm) each

LabelLabel

BIOFREEZE OVERNIGHT RELIEF 
menthol, unspecified form patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59316-005
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM0.3 g  in 6 g
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
GLYCERIN (UNII: PDC6A3C0OX)  
KAOLIN (UNII: 24H4NWX5CO)  
LAURALKONIUM CHLORIDE (UNII: 07HUP5A29X)  
LAVENDER OIL (UNII: ZBP1YXW0H8)  
MINERAL OIL (UNII: T5L8T28FGP)  
PETROLATUM (UNII: 4T6H12BN9U)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
TARTARIC ACID (UNII: W4888I119H)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
WATER (UNII: 059QF0KO0R)  
POLYACRYLIC ACID (450000 MW) (UNII: KD3S7H73D3)  
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
Product Characteristics
Color    Score    
ShapeRECTANGLESize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59316-005-036 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)02/01/2022
2NDC:59316-005-044 in 1 CARTON02/01/2022
26 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01702/01/2022
Labeler - RB Health (US) LLC (081049410)

Revised: 12/2023
Document Id: 0c66fe5b-db9f-d667-e063-6394a90a8ce6
Set id: 07be6e88-1850-4d6a-946d-f03830b8c4a2
Version: 3
Effective Time: 20231213
 
RB Health (US) LLC