Panama Jack
FDA Label NDC 58443-0179

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Prime Enterprises, Inc. for the product Panama Jack (NDC 58443-0179). 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 principal display panel - 30ml  bottle label, purpose, inactive ingrediets, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Principal Display Panel - 30Ml  Bottle Label

Principal Display Panel (30 mL Bottle Label)

Principal Display Panel (30 mL Bottle Label)

Panama Jack

SUNSCREEN

LOTION

1 FL OZ (30mL)

30 BROAD SPECTRUM SPF 30

CLEAR ZINC

WATER RESISTANT (80 MINUTES)

Purpose

Sunscreen

Inactive Ingrediets

Aluminium Starch Octenylsuccinate, Bis-PEG-12 Dimethicone Beeswax, Cetyl PEG/PPG-10/1 Dimethicone, Decyl Glucoside, Diazolidinyl Urea, Diisodecyl Adipate, Disodium EDTA, Glycerin, Hexyl Laurate, Hydrogenated Castor Oil, Methylparaben, Mineral Oil, Polyethylene, Polyglyceryl-4 Isostearate, Propylene Glycol, Propylparaben, Silica, Sodium Chloride, Tocopheryl Acetate, Triethoxycaprylysilane, Water

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