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UNNAPLAST with CALAMINE

Medically reviewed on September 30, 2016

Dosage form: paste
Ingredients: ZINC OXIDE 5mg in 1cm2, FERRIC OXIDE RED 0.2mg in 1cm2
Labeler: Pharmaplast SAE
NDC Code: 28691-2501

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

UNNAPLAST

Drug facts:

Active Ingredients

Zinc Oxide 25%
Calamine 1%

Purpose

Skin Protectant

Uses
  • Dries the oozing and weeping of poison ivy, poison oak, or poison sumac.
  • Ideal for managing extremities (e.g., varicose ulcers) requiring protection and support.

Warning
  • For external use only
  • If condition worsens or does not improve within 7 days, consult a doctor.
  • Avoid contact with eyes.

Keep Out of Reach of Children Section

• Keep this and all medicines out of children's reach.

Inactive Ingredients:
  • Carboxy methyl cellulose
  • Glycerol
  • Purified water

Directions
  1. Begin bandaging at base of toes, without pressure, keeping foot and leg at right angle. Continue bandaging beyond ankle, doubling back to ensure molding to contours of leg
  2. Continue bandaging to just below the knees.
  3. Apply an elastic adhesive bandage.

PRINCIPAL DISPLAY PANEL

Unnaplast™
Compression Plus occlusion
result in increased healing rate.
7.5 cm x 9.14 mts
10 cm x 9.14 mts

UNNAPLAST WITH CALAMINE 
zinc oxide and calamine paste
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:28691-2501
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (ZINC OXIDE) ZINC OXIDE5 mg  in 1 cm2
FERRIC OXIDE RED (FERRIC OXIDE RED) FERRIC OXIDE RED0.2 mg  in 1 cm2
Inactive Ingredients
Ingredient NameStrength
CARBOXYMETHYLCELLULOSE 
GLYCERIN 
WATER 
Packaging
#Item CodePackage Description
1NDC:28691-2501-11 POUCH in 1 BOX
16855 cm2 in 1 POUCH
2NDC:28691-2501-21 POUCH in 1 BOX
29140 cm2 in 1 POUCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34701/01/2014
Labeler - Pharmaplast SAE (557735337)
Establishment
NameAddressID/FEIOperations
Pharmaplast SAE557735337MANUFACTURE(28691-2501)

 
Pharmaplast SAE

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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