CALAMINE PLUS- calamine plus pramoxine hcl aerosol, spray 
Chain Drug Marketing Association Inc

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Quality Choice Calamine Plus Spray

Active ingredients

Calamine 8%

Pramoxine HCI 1%

Purpose

Skin protectant

External analgesic

Uses

temporarily relieves pain and itching associated with:

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. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.

When using this product

  • do not get into eyes
  • ask a doctor before using on children under 2 years of age

Stop use and ask a doctor if

  • condition worsens
  • symptoms last more than 7 days or clear up and occur again in a few days

Keep out of the reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other Information

store between 20° to 25°C (68° to 77°F)

Inactive ingredients

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

Questions?

Call 1-866-964-0939

Principal Display Panel

QC

QUALITY CHOICE

No-Rub

NO-RUB

Calamine

Plus Spray

Calamine 8% / Skin Protectant

Pramoxine HCI 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)

label

CALAMINE PLUS 
calamine plus pramoxine hcl aerosol, spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83324-242
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FERRIC OXIDE RED (UNII: 1K09F3G675) (FERRIC OXIDE RED - UNII:1K09F3G675) FERRIC OXIDE RED5 mg  in 1 g
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE10 mg  in 1 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE79.5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
ISOBUTANE (UNII: BXR49TP611)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
OLEYL ALCOHOL (UNII: 172F2WN8DV)  
SORBITAN TRIOLEATE (UNII: QE6F49RPJ1)  
ALCOHOL (UNII: 3K9958V90M)  
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83324-242-41116 g in 1 CANISTER; Type 0: Not a Combination Product06/07/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01706/07/2024
Labeler - Chain Drug Marketing Association Inc (011920774)

Revised: 6/2024
Document Id: 1a3f8151-5e4a-aa44-e063-6394a90a4f5b
Set id: 1a3f8819-58cf-8923-e063-6394a90a37af
Version: 1
Effective Time: 20240607
 
Chain Drug Marketing Association Inc