OTC Medication Information: Vanicream Anti-perspirant/Deodorant

VANICREAM ANTI-PERSPIRANT/DEODORANT- aluminum zirconium trichlorohydrex gly stick
Pharmaceutical Specialties, Inc.

Drug Facts

Active ingredient

Aluminum zirconium trichlorohydrex gly 20% (anhydrous)

Purpose

antiperspirant

Uses

  • reduces underarm wetness
  • 24 hour extra effective protection

Warnings

For external use only

Do not use on broken skin

Ask a doctor before use if you have kidney disease

Stop use if rash or irritation occurs

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions

apply to underams only

Other information

Store at room temperature

Inactive ingredients

cyclopentasiloxane, hydrogenated poly(C6-14 olefin), stearyl alcohol, phenyl trimethicone, hydrogenated castor oil, cetyl alcohol, silica

*To learn more about our products and ingredients, visit www.vanicream.com or call 1-800-325-8232.

Dist. by PHARMACEUTICAL SPECIALTIES, INC.

Rochester, MN 55901 U.S.A.

Made in Canada

Vanicream is a trademark, or registered trademark, of Pharmaceutical Specialties, Inc. in the U.S. or other countries.

KD21A

NDC 45334-305-02

DERMATOLOGIST TESTED

VANICREAM™

Anti-perspirant/Deodorant

Free of dyes, fragrance, masking fragrance, lanolin, parabens & formaldehyde releasers

FOR SENSITIVE SKIN

Net Wt 2.25 oz (64 g)

label
(click image for full-size original)
VANICREAM ANTI-PERSPIRANT/DEODORANT
aluminum zirconium trichlorohydrex gly stick
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:45334-305
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY (ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY) ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY 12.8 g in 64 g
Inactive Ingredients
Ingredient Name Strength
PHENYL TRIMETHICONE
HYDROGENATED CASTOR OIL
CETYL ALCOHOL
SILICON DIOXIDE
CYCLOMETHICONE 5
HYDROGENATED POLY(C6-14 OLEFIN; 6 CST)
STEARYL ALCOHOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:45334-305-02 64 g in 1 CONTAINER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC Monograph Drug M019 11/11/2016
Labeler — Pharmaceutical Specialties, Inc. (076499557)

Revised: 10/2023 Pharmaceutical Specialties, Inc.

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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