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Peviderm Pramoxine Hydrocholride 1%

Dosage form
LOTION
Labeler
Stratus Pharmaceuticals Inc
Label updated
2024-11-07
Retrieved
2026-09-07
Active ingredients
Pramoxine Hydrochloride
View original label and images on DailyMed ↗
Label information

Drug Facts

Active ingredient

Pramoxine Hydrochloride 1%

Purpose

External Analgesic

Uses
  • for the temporary relief of pain and itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites, minor skin irritations and rashes due to poison ivy, poison oak, or poison sumac
Warnings

for external use only

When using this product

  • avoid contact with eyes

Stop use and ask a doctor if

  • condition worsens
  • symptoms persist for more than 7 days or clear up and occur again within a few days

Label information

If pregnant or breast-feeding, ask a health professional before use

Label information

Keep out of reach of children.

If swallowed, get medical help or contact Poison Control Center immediately

Directions
  • to open, hold cap tightly and turn pump counter-clockwise

Adults and children 2 years of age and older:

  • apply to affected area not more than 3 to 4 times daily

Children under 2 years of age:

  • consult a doctor
Other information
  • Store at 20°C to 25°C (68°F to 77°F) [See USP Controlled Room Temperature]
Inactive ingredients

Benzyl Alcohol, Carbomer 940, Cetyl Alcohol, Dimethicone, Glyceryl Stearate, Isopropyl Myristate, Petrolatum, PEG-8 Stearate, PEG-100 Stearate, Purified Water, Sodium Hydroxide, Stearic Acid.

Questions or comments?

Call us at 1-800-442-7882

Label information

Distributed by:
STRATUS
PHARMACEUTICALS INC
Miami, Florida 33186

PRINCIPAL DISPLAY PANEL - 222 mL Bottle Box

NDC 58980-913-80

Steroid-Free & Fragrance-Free

PEVIDERM™
PRAMOXINE HYDROCHLORIDE 1%

ITCH RELIEF FOR SENSITIVE SKIN

EXTERNAL
ANALGESIC LOTION

Moisturizes and gently relieves
itch associated with:
Eczema and
Dry Sensitive Skin

Net 7.5 fl oz (222 mL)

[Image in the official label — see DailyMed source]

DailyMed Set ID: 680b40fa-1922-443a-a4b0-7c3f6a2b847d · Version 2
NDC: 58980-913