Celadrin

Manufacturer
Lifetech Resources, LLC
Effective date
2023-11-06
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:21:43

Label at a glance#

ProductCeladrin
Active ingredientMENTHOL
Label structure11 sections

Dosage and administration

Adults and children 2 yrs. of age and older . Apply to affected area not more than 3 to 4 times per day. Children under 2 yrs. of age: consult a physician.

Storage and handling

Store in a cool, dry place.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol (1.25%)

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Indications

INDICATIONS & USAGE SECTION

For temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises and sprains.

Warnings

WARNINGS SECTION

  • For external use only.

OTC - WHEN USING SECTION

  • Avoid contact with eyes.
  • 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 product and consult a physician.
  • Do not apply to wounds or damaged skin.
  • Do not bandage tightly.

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 2 yrs. of age and older. Apply to affected area not more than 3 to 4 times per day. Children under 2 yrs. of age: consult a physician.

Other Information

STORAGE AND HANDLING SECTION

Store in a cool, dry place.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Benzyl Alcohol, Butylparaben, Carbomer, Celadrin ®(a proprietary blend of esterified fatty acid carbons), Ethylparaben, Glycerin, Glyceryl Stearate, Isobutylparaben, Lecithin, Methylparaben, Olea Europaea (Olive) Fruit Oil, PEG-100 Stearate, Peppermint Oil, Phenoxyethanol, Potassium Hydroxide, Propylparaben, Tocopheryl Acetate, Water

Questions?

OTC - QUESTIONS SECTION

800-323-1688

SPL UNCLASSIFIED SECTION

Distributed by:Imagenetix, Inc. San Diego, Ca. 92127

www.celadrin.com

PRINCIPAL DISPLAY PANEL - 170 G Jar Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CLINICALLY TESTED • SHOWN TO WORK

FAST ACTING
celadrin
®

A D V A N C E D
JOINT & MUSCLE
PAIN RELIEVING CREAM

NET WT.
6 FL. OZ
(170 G)

OFFICIAL
PRODUCT

TOPICAL
ANALGESIC

Principal Display Panel - 170 G Jar Carton
Principal Display Panel - 170 G Jar Carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
65643-406-012023-11-01C16284748780-1956f9ecf-c498-621f-e053-dbdaa90a74adLifetech (as CMO) - Celadrin (65643-406)
65643-406-012019-10-21C16284748780-1956f9ecf-c498-621f-e053-dbdaa90a74adLifetech (as CMO) - Celadrin (65643-406)

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
MentholACTIVE INGREDIENTL7T10EIP3A1
MentholACTIVE MOIETYL7T10EIP3A1

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65643-40665643-406-01

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
WATER059QF0KO0RIACT
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
097fc533-6cd1-97ec-e063-6294a90a10aa36e010ac-556f-487a-a246-a932d5b426362023-11-06WarningsExact identifier
spl id: 097fc533-6cd1-97ec-e063-6294a90a10aa
spl set id: 36e010ac-556f-487a-a246-a932d5b42636

Reported adverse events (FAERS/openFDA)#

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