LILAS Feminine Pain Relief Patch

Manufacturer
Lilas Wellness, Inc.
Effective date
2022-06-20
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:49:52

Label at a glance#

ProductLILAS Feminine Pain Relief Patch
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure10 sections

Indications and uses

For temporary relief of minor aches and pains associated with: •menstrual cramps  •lower pelvic pain  •backache  •leg cramps  •sprains  •strains

Dosage and administration

adults and children 12 years of age and older apply to the affected area no more than 2 times daily dry the skin at application area before applying the patch open pouch & remove patch peel of protective film and apply sticky side to affected area children under 12 years of age consult a doctor

Storage and handling

Store at room temperature below 80°F (27ºC)

Label contents#

Full prescribing information#

Active Ingredients (In each patch)

OTC - ACTIVE INGREDIENT SECTION

Menthol 10.0%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

For temporary relief of minor aches and pains associated with:
•menstrual cramps  •lower pelvic pain  •backache  •leg cramps  •sprains  •strains

Warnings

WARNINGS SECTION

For external use only            Use only as directed

Do not use

• on wounds or damaged skin            • with a heating pad

Ask a doctor before use if you have 

• redness over affected area

When using this product

• avoid contact with the eyes, mucous membranes and rashes            • do not bandage tightly

Stop use or ask a doctor if
• condition worsens or symptoms persists for more than 7 days or clear up and occur again within a few days
• abnormal skin irritation occurs after usage

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 12 years of age and older apply to the affected area no more than 2 times daily
  • dry the skin at application area before applying the patch
  • open pouch & remove patch
  • peel of protective film and apply sticky side to affected area
  • children under 12 years of age consult a doctor

Other Information

STORAGE AND HANDLING SECTION

Store at room temperature below 80°F (27ºC)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

• adhesive plaster  • eucalyptus oil

Questions?

OTC - QUESTIONS SECTION

Call 1-833-400-4102

SPL UNCLASSIFIED SECTION

Your Natural Alternative to Pain Killers

Where To Use
Apply one or more patches based on the size of the pain affected area. Each patch can be used for up to 12 hours.

Pregnant women should NOT use on their abdomen

Neck

Legs

Back

Made of 100% Essential Oils

All Natural

Fast Acting

Lasts up to 12h

Cruelty Free

Distributed By:
LILAS Wellness Inc

9450 SW Gemini Dr
PMB 38333
Beaverton, Oregon
97008-7105

Made in India
by NC-DL-378-A&U

www.lilaswellness.com

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PATCHESPATCHES

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72670-001-03LILAS Feminine Pain Relief Patch3 in 1 PACKAGEPATCH34
72670-001-03LILAS Feminine Pain Relief Patch1 in 1 POUCHPATCH14
72670-001-05LILAS Feminine Pain Relief Patch5 in 1 PACKAGEPATCH54
72670-001-05LILAS Feminine Pain Relief Patch1 in 1 POUCHPATCH14
72670-001-10LILAS Feminine Pain Relief Patch10 in 1 BOXPATCH104
72670-001-10LILAS Feminine Pain Relief Patch1 in 1 POUCHPATCH14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72670-001LILAS FEMININE PAIN RELIEF PATCH ( MENTHOL) PATCH [LILAS WELLNESS, INC.]4Legacy NDC, 6 package rows20220622_7343aa3e-5d32-4bce-be0d-32ba1f78db2b.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72670-00172670-001-10, 72670-001-05, 72670-001-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB
EUCALYPTUS OIL2R04ONI662IACT

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
716a40f6-e5af-4fa8-9954-d4ea3829a6747343aa3e-5d32-4bce-be0d-32ba1f78db2b2022-06-20WarningsExact identifier
spl id: 716a40f6-e5af-4fa8-9954-d4ea3829a674
spl set id: 7343aa3e-5d32-4bce-be0d-32ba1f78db2b

Reported adverse events (FAERS/openFDA)#

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