FDA.reportPublic FDA data

Ultra Vedic

Manufacturer
Pharmaneek, Inc.
Effective date
2023-01-18
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 23:53:23

Label at a glance#

ProductUltra Vedic
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure16 sections

Indications and uses

For temporary relief of minor aches and pains in lower back and abdomen associated with cramps.

Dosage and administration

For use by Adults and Children 12 year of age and older Apply to the affected area no more than 2 times a day Dry skin completely at application site area, before applying the patch Open pouch and remove patch Peel off protective film and apply sticky side to affected area If applied on hairy skin, remove gently using mild warm water Patch once used cannot be re-pasted or reused Dispose properly after use

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Feminine Pain Relief Patch

The unique combination of pain relievers on the transdermal patch relieve pain due to cramps.

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 10%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

For temporary relief of minor aches and pains in lower back and abdomen associated with cramps.

7bdf737e-figure-01
7bdf737e-figure-01

Warnings

WARNINGS SECTION

For External Use Only

Do not use otherwise than as directed.

Do not use

OTC - DO NOT USE SECTION

  • On open wounds, cuts, eyes, and face
  • With a heating pad

When using this product

OTC - WHEN USING SECTION

  • Avoid contact with eyes and mucous membranes
  • Do not bandage tightly

Ask Your Doctor Before Use if you have

OTC - ASK DOCTOR SECTION

  • redness over the affected area
  • have sensitive skin
  • are pregnant or breast-feeding

Stop Use and Ask Your Doctor

OTC - STOP USE SECTION

  • If condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days
  • If abnormal skin irritation occurs after usage

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, seek medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • For use by Adults and Children 12 year of age and older
  • Apply to the affected area no more than 2 times a day
  • Dry skin completely at application site area, before applying the patch
  • Open pouch and remove patch
  • Peel off protective film and apply sticky side to affected area
  • If applied on hairy skin, remove gently using mild warm water
  • Patch once used cannot be re-pasted or reused
  • Dispose properly after use

Other Information

SPL UNCLASSIFIED SECTION

  • Store at room temperature below 80°F (27°C)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Adhesive Plaster, Eucalyptus Oil

SPL UNCLASSIFIED SECTION

Distributed by:
Pharmaneek, Inc.
7345 Woodland Dr., Ste A,
Indianapolis, IN 46278
© 2018. Made in India. NC/DL-378-A&U

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Please Reseal After Opening


NDC: 72625-130-05

ULTRA VEDIC

Feminine Pain Relief Patch

Pack of 5 Patches
Soothe Period Cramps
Medicated Patch
Fast Acting
Apply for 8-12 Hours

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7bdf737e-figure-02

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72625-130-052025-01-30C16284748780-12cef2736-842d-d83d-e063-dadaa90ab31fUltra Vedic TM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72625-130-05Ultra Vedic1 in 1 PATCHPATCH15
72625-130-05Ultra Vedic5 in 1 CARTONPATCH55

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72625-130ULTRA VEDIC (FEMININE PAIN RELIEF) PATCH [PHARMANEEK, INC.]5Legacy NDC, 2 package rows20230121_86d0da3e-b83f-4829-9a9d-5903cb388d1e.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
72625-13072625-130-05

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 · Source PDF

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
9f6fa49b-3aaf-48ab-aba2-ac74f6cbb6cc86d0da3e-b83f-4829-9a9d-5903cb388d1e2023-01-18WarningsExact identifier
spl id: 9f6fa49b-3aaf-48ab-aba2-ac74f6cbb6cc
spl set id: 86d0da3e-b83f-4829-9a9d-5903cb388d1e

Reported adverse events (FAERS/openFDA)#

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