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GNP Caldyphen

Dosage form: lotion
Ingredients: ZINC OXIDE 80mg in 1mL, PRAMOXINE HYDROCHLORIDE 10mg in 1mL
Labeler: Amerisource Bergen
NDC Code: 24385-072

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.

GNP Caldyphen Lotion

Drug Facts

Active Ingredients

Calamine 8%

Pramoxine HCl 1%

Purpose

Skin Protectant

External analgesic

Uses

Dries the oozing and weeping, and temporarily relieves pain and itching of poison ivy, oak, and sumac or other skin irritations.

Warnings

For external use only. Use only as directed.

When using this product. Avoid contact with eyes and moucous membranes.

Stop ue and ask a doctor if

condition worsens. Symptoms last for more than 7days or clear up and occur again whitin a few days.

Keep out of reach of children.

In case of accidental ingestion, seek profesional assistance or contact a Poison Control Center immediately.

Directions

Adults and children 2 yr. of age and older. Shake well before using. Cleanse the skin with soap and water and let dry. Apply to the affected area using cotton or soft cloth, not more than 3 to 4 times daily as needed for comfort.

Children under 2 yrs. of age. Consult a doctor before use.

Inactive Ingredients

SD Alcohol 38B 2.5%, Camphor, Diazolidinyl Urea, Fragrances, Glycerin, Hydroxypropyl Methycelulose, Methylparaben, Polysorbate 80, Propylene Glycol, Propylparaben and Purified Water.

Other information

Store at room temperature 15-30C (59-86F)

Distributed by: AmerisourceBergen

1300 Morris drive, Chesterbrook, PA 19087

Questions or Comments?

1-800-662-3435    www.goodneighborpharmacy.com

Principal Display Panel

Good Neighbor Pharmacy   NDC 24385-072-82

Caldyphen Lotion

External Analgesic/Skin Protectant

Relieves ITCHING due to:

Poison Ivy          Insect Bites

Poison Oak         Minor Skin Irritations

6 FL OZS (177 ml)

GNP CALDYPHEN 
calamine and pramoxine hydrochloride lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24385-072
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (ZINC CATION) ZINC CATION80 mg  in 1 mL
PRAMOXINE HYDROCHLORIDE (PRAMOXINE) PRAMOXINE HYDROCHLORIDE10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
CAMPHOR (NATURAL) 
DIAZOLIDINYL UREA 
GLYCERIN 
HYDROXYPROPYL METHYLCELLULOSE E5 [II] 
METHYLPARABEN 
POLYSORBATE 80 
PROPYLENE GLYCOL 
PROPYLPARABEN 
WATER 
Packaging
#Item CodePackage Description
1NDC:24385-072-82177 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34701/01/2008
Labeler - Amerisource Bergen (007914906)

 
Amerisource Bergen

Medically reviewed on Jul 2, 2018

Further information

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

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