FDA.reportPublic FDA data

CBD UNLIMITED BALMX

Manufacturer
Velocity Production and Packaging
Effective date
2020-12-16
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:01:33

Label at a glance#

ProductCBD UNLIMITED BALMX
Active ingredientMENTHOL
Label structure9 sections

Indications and uses

TEMPORARY RELIEF FROM MINOR ACHES AND PAINS OF MUSCLES & JOINTS ASSOCIATED WITH: ARTHRITIS SIMPLE BACKACHE STRAINS SPRAINS

Dosage and administration

ADULTS AND CHILDREN 12 YEARS OF AGE & OLDER. RUB WELL ON AFFECTED AREAS NOT MORE THAN 3 TO 4 TIMES DAILY. FOR CHILDREN 12 YEARS OR YOUNGER, CONSULT A DOCTOR BEFORE USE.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT(S)

OTC - ACTIVE INGREDIENT SECTION

MENTHOL USP 1.25%

PURPOSE

OTC - PURPOSE SECTION

TOPICAL ANALGESIC

USES

INDICATIONS & USAGE SECTION

TEMPORARY RELIEF FROM MINOR ACHES AND PAINS OF MUSCLES & JOINTS ASSOCIATED WITH:

  • ARTHRITIS
  • SIMPLE BACKACHE
  • STRAINS
  • SPRAINS

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY.

DO NOT USE ON WOUNDS OR DAMAGED SKIN.

WHEN USING THIS PRODUCT:

  • AVOID CONTACT WITH THE EYES
  • DO NOT BANDAGE TIGHTLY

STOP USE AND ASK A DOCTOR IF CONDITION WORSENS, OR IF SYMPTOMS PERSIST FOR MORE THAN 7 DAYS OR CLEAR UP AND OCCUR AGAIN WITHIN A FEW DAYS.

IF PREGNANT OR BREAT-FEEDING, ASK A HEALTH PROFESSIONAL BEFORE USE.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

ADULTS AND CHILDREN 12 YEARS OF AGE & OLDER. RUB WELL ON AFFECTED AREAS NOT MORE THAN 3 TO 4 TIMES DAILY.

  • FOR CHILDREN 12 YEARS OR YOUNGER, CONSULT A DOCTOR BEFORE USE.

OTHER INFORMATION

OTHER SAFETY INFORMATION

THIS PRODUCT MAY CAUSE AN ALLERGIC REACTION FOR SOME INDIVIDUALS. TEST ON SMALL AREA BEFORE USE.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

ARNICA OIL, BEESWAX, CLOVE BUD OIL, GRAPESEED OIL, HEMP ISOLATE, HEMP SEED OIL, LAVENDER OIL, METHYLSULFONYLMETHANE (MSM), MCT COCONUT OIL, ORGANIC LEMONGRASS OIL, ORGANIC MORINGA OIL, SWEET BIRCH OIL.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b UC_CBDU BalmX_2oz01b UC_CBDU BalmX_2oz

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
72591-075472591-0754-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
ARNICA MONTANAO80TY208ZWIACT
YELLOW WAX2ZA36H0S2VIACT
CLOVEK48IKT5321IACT
GRAPE SEED OIL930MLC8XGGIACT
HEMPTD1MUT01Q7IACT
CANNABIS SATIVA SEED OIL69VJ1LPN1SIACT
LAVENDER OILZBP1YXW0H8IACT
DIMETHYL SULFONE9H4PO4Z4FTIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
WEST INDIAN LEMONGRASS OIL5BIA40E9EDIACT
MORINGA OLEIFERA SEED OILREM6A5QMC0IACT
METHYL SALICYLATELAV5U5022YIACT
MENTHOLL7T10EIP3AACTIB

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
d30bdf4f-636d-9f96-e053-2995a90ac68745a3f7c2-402b-4b19-b5f6-4f0a42ed48192021-12-13WarningsExact identifier
spl set id: 45a3f7c2-402b-4b19-b5f6-4f0a42ed4819

Reported adverse events (FAERS/openFDA)#

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