VIASOX (as PLD) - PAIN RELIEF GEL (ROLL ON) (82687-101) - DELIST

PAIN RELIEF by

Drug Labeling and Warnings

PAIN RELIEF by is a Otc medication manufactured, distributed, or labeled by VIASOX LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PAIN RELIEF ROLL ON- menthol gel 
VIASOX LTD

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VIASOX (as PLD) - PAIN RELIEF GEL (ROLL ON) (82687-101) - DELIST

ACTIVE INGREDIENT

MENTHOL 11%

PURPOSE

TOPICAL ANALGESIC

USE

FOR THE TEMPORARY RELIEF OF MINOR ACHES AND PAINS OF MUSCLES AND JOINTS ASSOCIATED WITH SIMPLE BACKACHE, STRAINS, BRUISES, AND SPRAINS

WARNINGS

FOR EXTERNAL USE ONLY.

DO NOT USE:

• DO NOT USE AROUND EYE AREA, ON OPEN WOUNDS, CUTS, DAMAGED OR INFECTED SKIN, MOUTH, GENITALS OR ANY OTHER MUCOUS MEMBRANE
• IF CONTACT OCCURS, FLUSH THOROUGHLY WITH WATER
• IF IRRITATION CONDITION WORSENS, OR IF SYMPTOMS PERSIST FOR MORE THAN 7 DAYS, DISCONTINUE USE OF THIS PRODUCT AND CONSULT A PHYSICIAN.

KEEP OUT OF REACH OF CHILDREN.

IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER.

DIRECTIONS:

ADULTS AND CHILDREN 2 YEARS OF AGE AND OLDER: APPLY TO AFFECTED AREA NOT MORE THAN 3 TO 4 TIMES DAILY. CHILDREN UNDER 2 YEARS OF AGE: CONSULT A PHYSICIAN.

INACTIVE INGREDIENTS:

ALOE BARBADENSIS LEAF JUICE, GLYCERIN, BENZOIC ACID, CAPRYLIC/CAPRIC TRIGLYCERIDES, PHENOXYETHANOL, CETEARETH-6 OLIVATE, POTASSIUM CETYL PHOSPHATE, DENATURED DEHYDRATED ALCOHOL 40B, WATER, ETHYHEXYLGLYCERIN, XANTHAN GUM

OTHER INFORMATION:

KEEP CAP TIGHTLY CLOSED. STORE IN A COOL, DRY PLACE.

QUESTIONS

IF YOU HAVE QUESTIONS OR CONCERNS PLEASE CALL+1 (855) 768-1227

WWW.VIASOX.COM

PAIN RELIEF  ROLL ON
menthol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82687-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	11 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)	Â
CETEARETH-6 OLIVATE (UNII: 8834VWF9MO)	Â
DEHYDRATED ALCOHOL (UNII: 3K9958V90M)	Â
XANTHAN GUM (UNII: TTV12P4NEE)	Â
BENZOIC ACID (UNII: 8SKN0B0MIM)	Â
WATER (UNII: 059QF0KO0R)	Â
ALOE VERA LEAF (UNII: ZY81Z83H0X)	Â
GLYCERIN (UNII: PDC6A3C0OX)	Â
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)	Â
PHENOXYETHANOL (UNII: HIE492ZZ3T)	Â
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)	Â

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82687-101-13	90 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	04/26/2022	12/31/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	04/26/2022	12/31/2023

Labeler - VIASOX LTD (240308383)

Revised: 3/2024

Document Id: 14bc78f3-c974-d45f-e063-6294a90aa9e5

34390-5

Set id: dd949b29-e5ba-6e0d-e053-2995a90a6025

Version: 3

Effective Time: 20240328

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