Allergy Relief
FDA Label NDC 36800-933

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Topco Associates Llc for the product Allergy Relief (NDC 36800-933). 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 active ingredient (in each capsule), purpose, uses, do not use, ask a doctor before use if you have, ask a doctor or pharmacist before use if you are, when using this product, if pregnant or breast-feeding,, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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Compare to Benadryl® Dye-Free LIQUI-GELS® active ingredient*

Allergy Relief

Diphenhydramine HCl 25 mg/Antihistamine

Dye-Free

temporarily Relieves:

Sneezing
Runny Nose
Itchy, Watery Eyes
Itchy Nose or Throat
Softgels

*This product is not manufactured or distributed by McNeil Consumer Healthcare, distributor of Benadryl®, or Catalent Pharma Solutions, Inc., owner of the registered trademark LIQUI-GELS®.

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