Azo Urinary Pain Relief Tablet
Product Images NDC 49973-247

7 FDA label images from I-health, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Azo Urinary Pain Relief (NDC 49973-247). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by I-health, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

49973 247 12

49973 247 12
Carton label for AZO Urinary Pain Relief Maximum Strength tablets, containing 12 tablets of Phenazopyridine Hydrochloride 99.5 mg. The label highlights it as a urinary pain relief product marketed by i-Health, Inc. The front panel emphasizes fast relief and maximum strength, while the back panel includes detailed drug facts, directions, warnings, and inactive ingredients.*
FDA Label Image

49973 247 24

49973 247 24
Packaging label for AZO Urinary Pain Relief Maximum Strength tablets containing Phenazopyridine Hydrochloride 99.5 mg. The label highlights it as a urinary pain relief product with 24 tablets per package. Distributed by i-Health, Inc., the label includes drug facts, directions, warnings, and other product information.*
FDA Label Image

Azo Upr 96 Insert Eng

Azo Upr 96 Insert Eng
Drug facts label for AZO Urinary Pain Relief Maximum Strength tablets containing 99.5 mg Phenazopyridine Hydrochloride. The label includes indications for urinary tract infection symptom relief and detailed warnings, directions, precautions, storage instructions, and tamper-evident information. It advises consulting a doctor for certain health conditions, proper use limits, and cautions about urine discoloration and potential staining.*
FDA Label Image

Azo Upr 96

Azo Upr 96
Packaging label for AZO Urinary Pain Relief Maximum Strength tablets containing 99.5 mg Phenazopyridine Hydrochloride. The label indicates 96 tablets per package, designed for oral use, and is marked Not For Retail Sale, intended for professional use by i-Health, Inc. The label highlights relief for urinary pain with strong UTI pain reliever claims and includes Drug Facts, directions, warnings, and inactive ingredients.*
FDA Label Image

Azo Upr 96 Insert Esp

Azo Upr 96 Insert Esp
Drug facts and instructions panel for AZO Urinary Pain Relief Maximum Strength 99.5 mg tablets. The text is in Spanish and includes warnings, usage instructions for adults and children, additional safety information, storage directions, and caution about potential product staining and interference with lab tests. It advises consulting a doctor before use in certain conditions and provides a contact number for adverse reaction reporting.*
FDA Label Image

Upr English Insert (Azo Upr Insert Eng)

Upr English Insert (Azo Upr Insert Eng)
AZO Urinary Pain Relief Maximum Strength tablets label with active ingredient Phenazopyridine Hydrochloride 99.5 mg. The label includes usage warnings, directions for use in adults and children 12 years and older, and precautionary information. It also displays a manufacturer coupon for $1.00 off one AZO product, along with promotional text for other AZO products such as AZO Cranberry, AZO Test Strips, and AZO Yeast Plus, provided by the labeler i-Health, Inc.*
FDA Label Image

Upr Spanish Insert (Azo Upr Insert Esp)

Upr Spanish Insert (Azo Upr Insert Esp)
Packaging label for AZO Urinary Pain Relief Maximum Strength tablets containing 99.5 mg of Phenazopyridine Hydrochloride. The label includes product name, strength, dosage form as tablets, and is labeled for human OTC use. It shows the labeler as i-Health, Inc., and includes instructions, warnings, and usage information in Spanish. Also featured is a coupon offering $1 off on any one AZO product.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.