POISON OAK- hydrocortisone, phenol gel 
DeMartini Spring Hill Pharmacy, Inc.

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DeMartini (as PLD) - POISON OAK gel (57479-101) - DELIST

HYDROCORTISONE (1% W/W)

PHENOL (0.5%)

PURPOSE

EXTERNAL ANALGESIC

ASTRINGENT

USES: POISON OAK, POISON SUMAC, POISON IVY, MOSQUITO BITES, OTHER ALLERGIC RASHES.

WARNINGS: FOR EXTERNAL USE ONLY. DO NOT USE ON EEP OR PUNCTURE WOUNDS, ANIMAL BITES, OR SERIOUS BURNS.

KEEP OUT OF REACH OF CHILDREN. IN CASE OF OVERDOSE, GET MEDICAL HELP ORCONTACT A POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS FOR USE: APPLY DIRECTLY TO THE RASH AREA 3 TO 5 TIMES DAILY OR AS NEEDED FOR THE RELIEF OF ITCHING, REDNESS OR WEEPING.

INACTIVE INGREDIENTS:  Alcohol Denat, Acrylates/C10-30, Alkyl Acrylate Crosspolymer, Aloe Vera Gel, Benzyl Alcohol, Blue 6, Citrus Medica Limonum (Lemon) Juice Extract, Hamamelis Virginiana, Potassium Hydroxide, Water

When using this product
• Avoid getting in eyes or mucus membranes. If contact occurs rinse thoroughly with water.
• Discontinue use if allergic to any of the components.

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.

If pregnant or breast feeding, ask a health professional before use.

Posion Oak Gel Label

POISON OAK 
hydrocortisone, phenol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57479-101
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE1 g  in 100 g
PHENOL (UNII: 339NCG44TV) (PHENOL - UNII:339NCG44TV) PHENOL0.5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
D&C BLUE NO. 6 (UNII: 1G5BK41P4F)  
LEMON JUICE (UNII: AGN709ANTJ)  
WITCH HAZEL (UNII: 101I4J0U34)  
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:57479-101-13100 g in 1 TUBE; Type 0: Not a Combination Product11/29/201212/31/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01611/29/201212/31/2023
Labeler - DeMartini Spring Hill Pharmacy, Inc. (038273603)

Revised: 4/2024
 
DeMartini Spring Hill Pharmacy, Inc.