Active Ingredient
Pramoxine Hydrochloride 1.0% w/w
Reeses
FDA Label NDC 10956-799
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Reese Pharmaceutical Co for the product Reeses (NDC 10956-799). 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, purpose, uses, warnings, when using this product, stop use and ask a doctor if, keep out of the reach of children., direction, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
ANALGESIC
Uses
- Temporarily relieves itching
Warnings
For external use only
When Using This Product
- Avoid contact with eyes
Stop Use And Ask A Doctor If
- Condition worsens or does not improve within 7 days or clears up and reoccurs within a few days
Keep Out Of The Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Direction
- Adults: unfold wipe and cleanse the area by gently wiping or patting external area from front to back. Use each wipe only once and discard.
- Use up to 5 times daily.
- Children under 12: consult a doctor
Other Information
- Store at room temperature
- Discard within 2 months of opening
Inactive Ingredients
purified water, glycerin, propylene glycol, cocoamphodiacetate, polysorbate 20, aloe vera barbadensis leaf juice, citric acid, fragrance, diazolidinyl urea, iodopropynyl butylcarbamate.
Questions Or Comments?
1-800-321-7178
Images Of Representative Packaging
Image On Carton (Carton)
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