CALAMINE PLUS- calamine, pramoxine hydrochloride spray

Drug Labeling and Warnings

Drug Details [pdf]

Active ingredients

Calamine 8%

Pramoxine HCl 1%

Purposes

Skin Protectant

External analgesic

Uses

temporarily relieves pain and itching associated with:

• insect bites
• rashes
• minor skin irritations
• minor cuts
• dries the oozing and weeping of poison ivy, poison oak and poison sumac

Warnings

For external use only.

Flammable: Do not use while smoking or near heat or flame. Do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120°F.

When using this product

• do not get into eyes

Stop use and ask a doctor if

• conditions worsen or symptoms persist for more than 7 days
• symptoms clear up and occur again within a few days.

Keep out of reach of children.

If swallowed, get medical help or contact Poison Control Center (1-800-222-1222)

Directions

• Shake well before using
• Adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily
• cleanse the skin with soap and water
• let dry before use
• Children under 2 years of age: ask a doctor.

Other information

store at 20° to 25°C (68° to 77°F)

Inactive ingredients

benzyl alcohol, camphor, disteardimonium hectorite, hydrated silica, oleyl alcohol, SD Alcohol 40-B, sorbitan trioleate

Questions or comments?

Call 1-800-632-6900

Principal Display Panel - 116 g Can label

COMPARE TO the active ingredients in CALADRYL ® LOTION*

NDC: 30142-429-41

NO-RUB

Kroger ®

Calamine

Plus Spray

Calamine 8%

Skin Protectant

Pramoxine HCl 1%

External Analgesic

Relieves Itching From

Poison Ivy, Oak & Sumac,

& Insect Bites

Soothes Minor Skin

Irritations & Cuts

Shake Well Before Use

NET WT 4.1 OZ (116 g)

INGREDIENTS AND APPEARANCE

CALAMINE PLUS 
calamine, pramoxine hydrochloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 30142-429
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	79.6 mg  in 1 g
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056)	PRAMOXINE HYDROCHLORIDE	10 mg  in 1 g
FERRIC OXIDE RED (UNII: 1K09F3G675) (FERRIC OXIDE RED - UNII:1K09F3G675)	FERRIC OXIDE RED	0.4 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
HYDRATED SILICA (UNII: Y6O7T4G8P9)
SORBITAN TRIOLEATE (UNII: QE6F49RPJ1)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
BENZYL ALCOHOL (UNII: LKG8494WBH)
ALCOHOL (UNII: 3K9958V90M)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
OLEYL ALCOHOL (UNII: 172F2WN8DV)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 30142-429-41	116 g in 1 CAN; Type 0: Not a Combination Product	04/16/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	04/16/2026

Labeler - Kroger Company (006999528)