FDA.reportPublic FDA data

Roll Pain Away Lemongrass

Manufacturer
PROXIMITY CAPITAL PARTNERS LLC DBA ASUTRA | BioLyte Laboratories, LLC
Effective date
2026-06-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
monthly-update
Hydrated at
2026-07-17 21:34:34

Label at a glance#

ProductRoll Pain Away Lemongrass
Active ingredientCAPSAICIN
Label structure9 sections

Indications and uses

Temporarily relieves minor aches and pains of muscles and joints associated with: arthritis simple backache strains sprains bruises

Dosage and administration

Adults and children over 18 years: Apply to affected area. Massage into the painful area until thoroughly absorbed. Repeat as necessary but no more than 3 to 4 times daily. Wash hands with soap and water after applying Children 18 years and younger: Consult a doctor.

Storage and handling

Store in a cool, dry place Keep away from excessive heat or flame Tamper-evident for your protection. Use only if safety seal is intact.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Capsaicin .025%

Purpose

OTC - PURPOSE SECTION

Capsaicin .025%..................Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

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

  • arthritis
  • simple backache
  • strains
  • sprains
  • bruises

Warnings

WARNINGS SECTION

Use only as directed.

For external use only.

OTC - WHEN USING SECTION

When using this product:

  • avoid contact with eyes
  • do not apply to wounds or damaged skin
  • do not bandage tightly

OTC - STOP USE SECTION

Stop use and ask doctor if:

  • condition worsens
  • symptoms persist for more than 7 days, or clear up and reoccur again within a few days
  • redness is present
  • irritation develops

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If accidentally ingested, get medical help or contact Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children over 18 years:

  • Apply to affected area. Massage into the painful area until thoroughly absorbed. Repeat as necessary but no more than 3 to 4 times daily.
  • Wash hands with soap and water after applying

Children 18 years and younger:

  • Consult a doctor.

Other information

STORAGE AND HANDLING SECTION

  • Store in a cool, dry place
  • Keep away from excessive heat or flame
  • Tamper-evident for your protection. Use only if safety seal is intact.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Magnesium Chloride, C15-19 Alkane, Cetearyl Alcohol, Caprylic/Capric Triglycerides, Methylsulfonylmethane, Glycerin USP, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Co-polymer, Benzyl Alchol & Salicylic Acid & Glycerin & Sorbic Acid, Tocopheryl Acetate, Cymbopogon Flexuosus (Lemongrass) Oil

Questions or Comments?

OTC - QUESTIONS SECTION

888-819-6472; Monday-Friday, 9am-5pm CT; Report any serious side effects to number above

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 72683-011-01

Asutra*

Roll pain away

.025% Capsaicin

Pain RElief Gel

With Revitalizing Magnesium and Lemongrass

Paraben Free

Non-Toxic

Animal Test-Free and Vegan

3.4 oz | 96g

11

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130850072769127GTIN-13: 0850072769127
EAN-13: 0850072769127
GTIN-12: 850072769127
UPC-A: 850072769127
GTIN storage (14 digits): 00850072769127		Screenshot 2026-06-17 214151.jpg

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72683-01172683-011-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
C15-19 ALKANECI87N1IM01IACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
GLYCERINPDC6A3C0OXIACT
CETEARYL ALCOHOL2DMT128M1SIACT
CAPSAICINS07O44R1ZMACTIB
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
DIMETHYL SULFONE9H4PO4Z4FTIACT
SORBIC ACIDX045WJ989BIACT
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%)86FQE96TZ4IACT
BENZYL ALCOHOLLKG8494WBHIACT
MAGNESIUM CHLORIDE02F3473H9OIACT
WATER059QF0KO0RIACT
SALICYLIC ACIDO414PZ4LPZIACT
LEMONGRASS OIL5BIA40E9EDIACT

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
Roll Pain Away LemongrassCAPSAICINPROXIMITY CAPITAL PARTNERS LLC DBA ASUTRA547ef5c0-bc31-d83e-e063-6394a90abfa62026-06-17WarningsExact identifier
ndc (package): 72683-011-01
ndc (product): 72683-011
ndc11 (package): 72683001101
spl id: 547ef245-9c5a-2d51-e063-6294a90a5506
spl set id: 547ef5c0-bc31-d83e-e063-6394a90abfa6

Reported adverse events (FAERS/openFDA)#

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