Calamine, Pramoxind HCl

Lotion · Topical

Over the counter

Active ingredient

Active ingredients Calamine 8% Pramoxine HCl 1%

Purpose

Purpose Skin protectant External analgesic

Uses

Uses for the temporary relief of pain and itching associated with minor skin irritations and rashes due to poison ivy, poison oak, or poison sumac dries the oozing and weeping of poison: ■ ivy ■ oak ■ sumac

Warnings

Warnings For external use only

When using this product

When using this product do not get into eyes

Stop use and ask a doctor

Stop use and ask a doctor if condition worsens symptoms last more than 7 days or clear up and occur again within a few days

Keep out of reach of children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Directions shake well before applying wash affected area of skin 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: do not use, ask a doctor

Inactive ingredients

Inactive ingredients alcohol, benzyl alcohol, camphor, fragrance, hydroxypropyl methylcellulose, Lavandula angustifolia (lavender) oil, phenoxyethanol, polysorbate 80, propylene glycol, Rosmarinus officinalis (rosemary) leaf oil, water, xanthan gum

Questions?

Questions? 1-888-593-0593

Label text from the FDA structured product label by H E B (revised Jun 15, 2026). Long sections are shortened; the complete label is on DailyMed.

Active ingredients

Calamine, Pramoxind HCl NDC products (1)

NDCStrength & formLabelerType
37808-616Ferric Oxide Red 80 mg/mL; Pramoxine Hydrochloride 10 mg/mL
Lotion
H E BOTC MONOGRAPH DRUG

Frequently asked questions

What is Calamine, Pramoxind HCl used for?

Uses for the temporary relief of pain and itching associated with minor skin irritations and rashes due to poison ivy, poison oak, or poison sumac dries the oozing and weeping of poison: ■ ivy ■ oak ■ sumac

Who makes Calamine, Pramoxind HCl?

Calamine, Pramoxind HCl is listed by 1 labeler in the FDA NDC directory, including H E B.