CALDESENE MEDICATED PROTECTING- cornstarch and zinc oxide powder 
Insight Pharmaceuticals LLC

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Caldesene Medicated Protecting Powder

Drug Facts

Active ingredients

Cornstarch 81%

Zinc Oxide 15%

Purpose

Skin Protectant

Skin Protectant

Uses

Warnings

For external use only.

Do not use

on broken skin.

When using this product

  • avoid contact with eyes
  • keep away from face and mouth to avoid breathing it

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.

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

Directions

For diaper rash

For minor skin irritations

Other information 

Store at room temperature 15-25°C (59-77°F). 

See container bottom for lot number and expiration date.

Inactive ingredients

aloe vera gel, chamomile, fragrance, kaolin, tricalcium phosphate

Questions?

1-800-344-7239 www.caldesene.com

PRINCIPAL DISPLAY PANEL

Caldesene ®
by Boudreaux’s Butt Paste ®

Medicated Protecting Powder
Skin protectant / cornstarch 81%

and zinc oxide 15%




NET WT 5 OZ (142 g)

PRINCIPAL DISPLAY PANEL
Caldesene ®
by Boudreaux’s Butt Paste ®
Medicated Protecting Powder
Skin protectant / cornstarch 81%
and zinc oxide 15%



NET WT 5 OZ (142 g)

CALDESENE MEDICATED PROTECTING 
cornstarch and zinc oxide powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63736-306
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
STARCH, CORN (UNII: O8232NY3SJ) (STARCH, CORN - UNII:O8232NY3SJ) STARCH, CORN115 g  in 142 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE21 g  in 142 g
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CHAMOMILE (UNII: FGL3685T2X)  
KAOLIN (UNII: 24H4NWX5CO)  
TRICALCIUM PHOSPHATE (UNII: K4C08XP666)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63736-306-01142 g in 1 BOTTLE; Type 0: Not a Combination Product07/15/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01607/15/2017
Labeler - Insight Pharmaceuticals LLC (055665422)

Revised: 1/2024
Document Id: 79ee3486-1605-4f14-9f9a-be340efa48a6
Set id: ffc92a0f-a7cf-4a46-b2f1-089df2bbb96b
Version: 5
Effective Time: 20240126
 
Insight Pharmaceuticals LLC