OTC Medication Information: Head and Shoulders Calming Lavender Daily Hair and Scalp Conditioner

HEAD AND SHOULDERS CALMING LAVENDER DAILY HAIR AND SCALP CONDITIONER- pyrithione zinc lotion
The Procter & Gamble Manufacturing Company

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Facts

Active ingredient

Pyrithione zinc 0.5%

Purpose

Anti-dandruff

Uses

helps prevent recurrence of flaking and itching associated with dandruff.

Warnings

For external use only.

When using this product

  • avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

  • condition worsens or does not improve after regular use of this product as directed.

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

Directions

  • for best results use at least twice a week or as directed by a doctor.
  • apply to wet hair after shampooing by gently massaging into hair and scalp, rinse well.

Inactive ingredients

Water, stearyl alcohol, cetyl alcohol, stearamidopropyl dimethylamine, glutamic acid, dimethicone, fragrance, phenoxyethanol, benzyl alcohol, citric acid, sodium chloride, lavandula angustifolia (lavender) flower extract,methylchloroisothiazolinone, methylisothiazolinone.

Questions (or comments)?

1-800-723-9569

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL — 325 mL Tube Label

head &
shoulders ®

pyrithione zinc dandruff conditioner

CALMING LAVENDER

DAILY HAIR & SCALP

CALMING CONDITIONER

infused with LAVENDER + JASMINE ESSENCE

10.6 FL OZ (315 mL)

HS
(click image for full-size original)
HEAD AND SHOULDERS CALMING LAVENDER DAILY HAIR AND SCALP CONDITIONER
pyrithione zinc lotion
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-320
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PYRITHIONE ZINC (PYRITHIONE ZINC) PYRITHIONE ZINC 0.5 g in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER
STEARYL ALCOHOL
CETYL ALCOHOL
STEARAMIDOPROPYL DIMETHYLAMINE
GLUTAMIC ACID
DIMETHICONE
PHENOXYETHANOL
BENZYL ALCOHOL
CITRIC ACID MONOHYDRATE
SODIUM CHLORIDE
LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:69423-320-31 315 mL in 1 TUBE None
2 NDC:69423-320-38 380 mL in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final M032 08/06/2018 09/01/2024
Labeler — The Procter & Gamble Manufacturing Company (004238200)

Revised: 03/2023 The Procter & Gamble Manufacturing Company

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.

Terms of Use | Copyright © 2024. All Rights Reserved.