Webb Candy
FDA Label NDC 49701-9000
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Webb Candy for the product Webb Candy (NDC 49701-9000). 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 otc - active ingredient, otc - purpose, otc - ask doctor, otc - keep out of reach of children, dosage & administration, information for patients, inactive ingredient, otc - questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Otc - Ask Doctor
Otc - Keep Out Of Reach Of Children
Dosage & Administration
Information For Patients
Inactive Ingredient
Inactive Ingredients
POLYBUTENE, MINERAL OIL, ETHYLHEXYL PALMITATE,
PARAFFIN, CERESINE, MICROCRYSTALLINE WAX, BEES
WAX, FRAGRANCE, METHYLPARABEN, PROPYLPARABEN,
D AND C BLUE NO. 1 AL LAKE, TITANIUM DIOXIDE
Otc - Questions
1.800.999.9322 or Visit
hiyamints.com or
webbcandy.com
Package Label.Principal Display Panel
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