Glucosamine Cream Extra Strength Cream
FDA Label NDC 78983-101

7 label sections · Submitted to the FDA by Ideaz, Llc · Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Ideaz, Llc for the product Glucosamine Cream Extra Strength (NDC 78983-101). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding drug facts, active ingredient, purpose, keep out of reach of children., directions, inactive ingredient, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

ACtive Ingredient

Histamine Dihydrochloride 0.05%

Purpose

Topical Analgesic

Keep Out Of Reach Of Children.

If swallowed get medical help or contact a poison control center

Directions

For use by adults and children over 12 years:

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

Inactive Ingredient

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

Packaging

Label (Drnewtonsextrastrength)

Label (Drnewtonsextrastrength)

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