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Vanoxide Hc Package Insert

Status:
Prescription (Rx) Facts
Strength:
5 g/100 g, 0.5 g/100 g
Drug class:
Active ingredients:

Prescribing information (package insert) - Vanoxide Hc

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.

About this document

Source: FDA drug labeling via NLM DailyMed · View the label on DailyMed

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Drug information for Vanoxide Hc

Rx or OTC
Prescription (Rx)?
  • This drug is available only with a prescription from a licensed healthcare provider.
  • Rx
Drug class Corticosteroid
Active ingredients Benzoyl peroxide 5 g/100 g, Hydrocortisone 0.5 g/100 g
Dosage form Lotion
Route Topical
Marketing status not in the current FDA NDC Directory
Company (applicant) Summers Laboratories Inc
FDA approval UNAPPROVED DRUG OTHERUnapproved drug
Manufacturers 1 labelers list this drug on DailyMed
Packages (NDC)
Package
5 g/100 g, 0.5 g/100 g – 25 g in 1 bottle NDC 11086-032-01

Source: FDA drug labeling via NLM DailyMed, data as of October 31, 2026. FDA data (DailyMed, Orange Book, Drug Shortages, enforcement reports). Not a substitute for the advice of a doctor or pharmacist.