Glucosamine Cream EXTRA STRENGTH

Manufacturer
Q.A. Laboratories
Effective date
2022-01-17
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:47:34

Label at a glance#

ProductGlucosamine Cream EXTRA STRENGTH
Active ingredientHISTAMINE DIHYDROCHLORIDE
Label structure9 sections

Dosage and administration

For use by adults and children over 12 years: Apply to affected area not more than 3 to 4 times daily.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Histamine Dihydrochloride 0.05%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

Warnings For external use only

When using this product

  • Avoid contact with eyes
  • Do not bandage tightly

Do not use 

  • On wounds or damaged skin or if you are allergic to ingredients in this product.

Discontinue use and consult a physician if: Condition worsens or if symptoms persists for more than 7 days or clear up and occur again within a few days

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed get medical help or contact a poison control center

Directions

DOSAGE & ADMINISTRATION SECTION

For use by adults and children over 12 years:

Apply to affected area not more than 3 to 4 times daily.

INACTIVE INGREDIENT SECTION

Inactive ingredients Deionized water, cetearyl alcohol, emu oil, glycerine, ceteareth-20, glucosamine sulfate, dimethyl sulfone, caprylic capric triglyceride, phenoxyethanol, cetyl alcohol, methyl paraben, tocopherol acetate, butylene glycol, propylene glycol, chamomilla recutita flower extract, rosmarinus officinalis leaf extract, boswellia serrata extract, propyl paraben

SPL UNCLASSIFIED SECTION

Pain Relief On Contact

Dual Action Moisturizing Cream

Odorless, Greaseless, Stainless.

Made in USA

For re-orders call 800-280-5590

www.drnewtons.com

Distributed by

Dr. Newton's Naturals

26 Thomas Drive

Westbrook, ME 04092

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1542820histamine dihydrochloride 0.05 % Topical CreamPSN3
1542820histamine dihydrochloride 0.5 MG/ML Topical CreamSCD3
1542820histamine dihydrochloride 0.05 % Topical CreamSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52099-0008-32023-07-28C16284748780-10191ceaa-6646-198a-e063-dbdaa90aec3eGlucosamine Cream EXTRA STRENGTH

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52099-0008-3Glucosamine Cream EXTRA STRENGTH85 g in 1 TUBECREAM853

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52099-0008GLUCOSAMINE CREAM EXTRA STRENGTH (HISTAMINE DIHYDROCHLORIDE) CREAM [Q.A. LABORATORIES]3Legacy NDC, 1 package rows20220126_8f812286-cb6e-42ae-b141-c3a3e55ad2fc.zip

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52099-000852099-0008-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 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
1fac82ef-e65b-4cc5-b04c-4e2cf1c823c78f812286-cb6e-42ae-b141-c3a3e55ad2fc2022-01-17WarningsExact identifier
spl id: 1fac82ef-e65b-4cc5-b04c-4e2cf1c823c7
spl set id: 8f812286-cb6e-42ae-b141-c3a3e55ad2fc

Reported adverse events (FAERS/openFDA)#

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