CBD4 FREEZE PUMP VANISHING SCENT

Manufacturer
HMP BRANDS, LLC
Effective date
2020-10-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:32:50

Label at a glance#

ProductCBD4 FREEZE PUMP VANISHING SCENT
Active ingredientLIDOCAINE, MENTHOL
Label structure11 sections

Dosage and administration

adults and children over 12 years: Apply a thin layer to affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period. After applying, wash hands with soap and water Children 12 years or younger: ask a doctor

Storage and handling

Store at 68-77°F (20-25°F) in a dry place  Keep from freezing

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient                                        Purpose

Lidocaine HCI USP 4%.............................. Topical anesthetic

Menthol USP 1 % ....................................  Topical analgesic

Use

INDICATIONS & USAGE SECTION

Temporarily relieves minor pain.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

  • on large areas of the body or on cut, irritated or swollen skin.
  • on puncture wounds.
  • for more than one week without consulting a doctor.

OTC - WHEN USING SECTION

When using this product

  • Use only as directed.
  • Read and follow all directions and warnings on this label.
  • Rare cases of serious burns have been reported with products of this type.
  • Do not bandage tightly or apply local heat (such as heating pads) to the area of use or use with a medicated patch.
  • Avoid contact with eyes and mucous membranes.
  • A transient burning sensation may occur upon application but generally disappears in several days.

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • condition worsens.
  • redness is present.
  • irritation develops.
  • symptoms persist for more than 7 days or clear up and occur again within a few days.
  • You experience signs of skin injury, such as pain, swelling, or blistering where the product was applied.

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

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 over 12 years:

  • Apply a thin layer to affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period.
  • After applying, wash hands with soap and water

Children 12 years or younger: ask a doctor

Other information

STORAGE AND HANDLING SECTION

  • Store at 68-77°F (20-25°F) in a dry place 
  • Keep from freezing

Inactive ingredients

INACTIVE INGREDIENT SECTION

cetostearyl alcohol, citric acid, hemp extract(cannabidiol), light liquid paraffin, macrogol cetostearyl ether, methyl parahydroxybenzoate, peppermint oil, purified water, sodium citrate and white soft paraffin.

PRODUCT LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
4d7a96d5-8256-4268-9a6c-25ea66d321feProduct name120180814
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80875-421-602021-07-23C16284748780-1c7ccaba7-2745-fd44-e053-dadaa90aa01b507740f3-17d5-4acd-814e-75f5dcb372a0

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80875-421-60CBD4 FREEZE PUMP VANISHING SCENT60 g in 1 TUBECREAM601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80875-421CBD4 FREEZE PUMP VANISHING SCENT (LIDOCAINE, MENTHOL) CREAM [HMP BRANDS, LLC]1Legacy NDC, 1 package rows20201105_507740f3-17d5-4acd-814e-75f5dcb372a0.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
80875-421-60GM - Gram80875-4217198c278-6255-4531-809a-8b8e598f75e212021-04-08

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80875-42180875-421-60

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
fa4214b0-f0d6-43b4-a306-d276f8afc5c6507740f3-17d5-4acd-814e-75f5dcb372a02020-10-22WarningsExact identifier
spl id: fa4214b0-f0d6-43b4-a306-d276f8afc5c6
spl set id: 507740f3-17d5-4acd-814e-75f5dcb372a0

Reported adverse events (FAERS/openFDA)#

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