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Home > Drugs > Topical acne agents > Vanoxide-hc > Vanoxide HC Prescribing Information
Topical acne agents
https://themeditary.com/pro/vanoxide-hc-prescribing-information-14697.html

Vanoxide HC Prescribing Information

Drug Detail:Vanoxide-hc (Benzoyl peroxide and hydrocortisone topical [ ben-zoyl-per-ox-ide-and-hye-droe-kor-ti-sone-top-i-kal ])

Drug Class: Topical acne agents

Contents
Uses Warnings Before Taking Dosage Side effects Interactions

ACTIVE INGREDIENTS:

BENZOYL PEROXIDE 5%

HYDROCORTISONE 0.5%

Apply with caution on neck and/or other sensitive areas. There may be a slight transitory stinging or burning sensation on initial applications. Colored or dyed garments and linens may be bleached by the action of benzoyl peroxide. If irritation or sensitivity is
observed, discontinue use and consult your physician.

KEEP OUT OF REACH OF CHILDREN.

TO THE PHARMACIST:
Prior to dispensing, add powder content of vial* to lotion. Shake bottle thoroughly to disperse completely. After addition of powder, place expiration date of 3 months on the bottle.
*Benzoyl-Pak™

  • Keep away from eyes. FOR TOPICAL USE ONLY.Not for ophthalmic, oral or intravaginal use.
  • Shake well before using.
  • Keep tightly closed.
  • Store at room temperature. 20°-25° C (68°-77° F). Do not freeze.

VHC-25G-carton

VHC-25G-label

VANOXIDE HC
benzoyl peroxide, hydrocortisone lotion
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:11086-032
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE5 g in 100 g
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE0.5 g in 100 g
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11086-032-0125 g in 1 BOTTLE; Type 0: Not a Combination Product11/01/2009
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other11/01/2009
Labeler - Summers Laboratories Inc (002382612)

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