POST TREATMENT BALM- hydrocortisone cream

Post Treatment Balm by

Drug Labeling and Warnings

Post Treatment Balm by is a Otc medication manufactured, distributed, or labeled by Allure Labs Inc., Allure Labs. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient: Hydrocortisone 1%

PURPOSE

Purpose: Anti-itch

INDICATIONS & USAGE

Uses:

• Promotes healing of itchy skin.
• Keeps skin hydrated.

WARNINGS

Warnings:

• For external use only.
• Ask a doctor if bleeding occurs or conditions worsens.
  

DO NOT USE

Do not use - If rashes appear on skin.

WHEN USING

When using this Product:

• Avoid contact with the eyes, lips and mouth.
• Do not use more than directed unless told to do so by a doctor.
  

STOP USE

Stop use and ask a doctor - If conditions worsens.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children:

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

DOSAGE & ADMINISTRATION

Directions:

• Apply to affected area not more than 3 to 4 times daily or as directed by your skin care professional.
  

INACTIVE INGREDIENT

Inactive Ingredients: Petrolatum, Carthamus Tintorius (Safflower) seed oil, Tocopheryl Acetate, Zinc Oxide, Titanium Dioxide, Ubiquinone, Glycosaminoglycans, PEG-8, Tocopherol, Ascorbyl Palmitate, Ascorbic Acid, Citric Acid, Caprylic/Capric Triglyceride, Triethoxycaprylylsilane, Dimethicone, Polymethylsilsesquioxane.

PRINCIPAL DISPLAY PANEL

Manufactured for

DermaQuest Inc.

Hayward, CA 94544

1272 GK, NL Made in USA

dermaquestinc.com

INGREDIENTS AND APPEARANCE

POST TREATMENT BALM 
hydrocortisone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62742-4077
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ)	HYDROCORTISONE	1 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
PETROLATUM (UNII: 4T6H12BN9U)
SAFFLOWER OIL (UNII: 65UEH262IS)
ACETATE ION (UNII: 569DQM74SC)
ZINC OXIDE (UNII: SOI2LOH54Z)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
UBIDECARENONE (UNII: EJ27X76M46)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
TOCOPHEROL (UNII: R0ZB2556P8)
ASCORBYL PALMITATE (UNII: QN83US2B0N)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
DIMETHICONE (UNII: 92RU3N3Y1O)
POLYMETHYLSILSESQUIOXANE (11 MICRONS) (UNII: Z570VEV8XK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62742-4077-1	56.7 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	05/12/2015

Labeler - Allure Labs, Inc (926831603)