Zax's Aches & Pain Cream/Creme

Manufacturer
Canadian Custom Packaging Company
Effective date
2024-12-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:42:35

Label at a glance#

ProductZaxs Aches and Pain
Active ingredientCAPSICUM, MENTHOL, METHYL SALICYLATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Capsicum 0.13%

Methyl Salicylate 10.5%

Menthol 5%

OTC - PURPOSE SECTION

Topical Analgesic

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints associated with: Simple backache, Arthritis, Strains, Bruises, Sprains. Penetrating pain relief.

DOSAGE & ADMINISTRATION SECTION

For use by Adults and Children over 12 years of age: Apply a thin layer to affected area, not more than 4 times a day. Rub and massage into skin until solution vanishes. Always wash hands after applying. Store in airtight, light resistant container at room temperature.

WARNINGS SECTION

• For external use only.

•Allergy alert: If allergic to aspirin or salicylates, consult a physician before use.

•When using this product, use only as directed. Make sure you understand directions and warnings on label before use.

°Rare case of burns have been reported with products of this type.

°Do not apply with external heat (such as electric heating pad) or bandage tightly.

°Do not apply to wounds or damaged skin, or irritated skin.

°If you are allergic to any ingredient in this product, do not use. Avoid contact with eyes and mucous membranes.

•If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician.

•Stop use if: Redness is present, irritation develops, you experience pain, swelling or blistering where product is applied.

•Consult a physician if you are breastfeeding or pregnant before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, consult a Poison Control Centre immediately.

INACTIVE INGREDIENT SECTION

Aqua, Butyrospermum Parkii (Shea Butter) Extraxt, Caprylic/capric triglyceride, Caprylyl Glycol, Camphor, Carbomer copolymer, Ceteareth-20, Cetearyl Alcohol, Cetyl Alcohol, Eucalyptus Leaf Oil, Glycerin, Mentha piperita (Peppermint) oil, Phenoxyethanol, Polysorbate 20, Sodium Hydroxide, Sorbic acid, Xanthan Gum

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Tube Label Tube LabelTube Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2585453capsicum extract 0.13 % / menthol 5 % / methyl salicylate 10.5 % Topical CreamPSN2
2585453Capsicum extract 1.3 MG/ML / menthol 50 MG/ML / methyl salicylate 105 MG/ML Topical CreamSCD2
2585453capsicum extract 0.13 % / menthol 5 % / methyl salicylate 10.5 % Topical CreamSY2

DailyMed Pharmacologic Classes#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54291-054-01Zaxs Aches and Pain120 g in 1 TUBECREAM1202

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54291-054ZAXS ACHES AND PAIN (CAPSICUM, METHYL SALICYLATE, MENTHOL) CREAM [CANADIAN CUSTOM PACKAGING COMPANY]21 package rows20241213_cff970a5-160e-79e1-e053-2995a90a6ff4.zip

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54291-05454291-054-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 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
29032114-f088-cdc0-e063-6294a90a302fcff970a5-160e-79e1-e053-2995a90a6ff42024-12-11WarningsExact identifier
spl id: 29032114-f088-cdc0-e063-6294a90a302f
spl set id: cff970a5-160e-79e1-e053-2995a90a6ff4

Reported adverse events (FAERS/openFDA)#

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