Dr Bump gel 4

Manufacturer
CA-BOTANA INTERNATIONAL
Effective date
2025-07-04
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 20:36:11

Label at a glance#

ProductDr Bump gel 4
Active ingredientMENTHOL
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Menthol 5% Topical Analgesic

Other Safety Information

Protect this product from excessive heat and direct sun

OTC - ASK DOCTOR

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if redness is present.irritation develops. conditions worsens or symtoms persist more than 7 days. symtoms clear up and occur again within a few days

OTC - PURPOSE SECTION

Uses: for temporary relief of minor aches and pains of muscles and joints associated with. simple aches. back aches. arthritis.strains.bruises.sprains.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Aesculus hippocastanum (Horse Chestnut), Aloe barbadensis miller, Aloe barbadensis miller (Aloe Vera), Amonium Acrylcydimethyltaurate/VPCcopolymer, Arnica montana (Arnica), Bromelain, Butylene Glycol, Capsicum annum (Capsicum), Chamaemelum nobile (Chamomile), Ethyl alcohol, Eucalyptus globules (Eucaliptus) oil, FD&C Green # 3, Glucosamine Sulfate, Harpagophytum procumbens (Devil’s Claw), Melissa officinalis (Lemon Balm), Methyl Sulfonyl Methane (MSM), Polysorbate-60, Potassium Sorbate, Purified Water, Rosmarinus officinalis (Rosemary), Salix alba (Willow Bark), Edetic Acid, Tilia cordata (Linden), Xanthan Gum

Warnings

WARNINGS SECTION

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

Dosage & Admnistration

DOSAGE & ADMINISTRATION SECTION

External topical analgesic Topical massage gel no more than 4 times daily

Indications & usage

INDICATIONS & USAGE SECTION

Apply generous amount of gel directly affected area massage into painful area until thoroughly absorbed into skin

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
35192-05235192-052-18

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 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
4b344fd9-b4ac-c8fd-e063-6394a90a55a7e847bf6b-b505-2253-e053-2995a90a5eab2026-02-19WarningsExact identifier
spl set id: e847bf6b-b505-2253-e053-2995a90a5eab

Reported adverse events (FAERS/openFDA)#

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