SprayPain Away Lavender

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 21:34:32

Label at a glance#

ProductSprayPain Away Lavender
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 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 a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults 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

Water, Magnesium Chloride, Polysorbate 20, Caprylic/Capric Triglyceride, Lavandula Augustifolia (Lavender) 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:

72683-006-01

Asutra*

Spray

pain

away

Capsaicin .025%

Pain Relieving Spray

Refreshing Magnesium Oil

4 fl. oz. | 118 ml.

Paraben Free

Animal Test-Free PETA Vegan

11

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72683-01272683-012-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
SprayPain Away LavenderCAPSAICINProximity Capital Partners LLC dba Asutra547e2167-ade0-ac7e-e063-6294a90a18ea2026-06-17WarningsExact identifier
ndc (package): 72683-012-01
ndc (product): 72683-012
ndc11 (package): 72683001201
spl id: 547e2ce8-374d-c164-e063-6294a90add75
spl set id: 547e2167-ade0-ac7e-e063-6294a90a18ea

Reported adverse events (FAERS/openFDA)#

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