Scalpicin® 2 in 1

Scalpicin by

Drug Labeling and Warnings

Scalpicin by is a Otc medication manufactured, distributed, or labeled by Reckitt Benckiser LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SCALPICIN  2 IN 1- salicylic acid liquid 
RB Health (US) LLC

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.

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Scalpicin®
2 in 1

Drug Facts

Active ingredient

Salicylic acid 3%

Purpose

Anti-dandruff liquid

Uses

  • controls the symptoms of dandruff
  • helps stop scalp itching, irritation, redness and flaking associated with seborrheic dermatitus and psoriasis

Warnings

For external use only

Flammable. Keep away from fire, flame or heat.

When using this product avoid contact with the 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 out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • apply to affected areas one to four times daily or as directed by a doctor
  • twist the flow-control cap to open
  • if using after shampooing, towel dry hair
  • apply from bottle directly to scalp, massage in
  • to avoid running or dripping, do not squeeze bottle too hard

Other information

  • store at 20-25°C (68-77°F)
  • protect from humidity

Inactive ingredients

alcohol denat., water, propylene glycol, menthol

Questions?

1-888-963-3382 You may also report side effects to this phone number.

Distributed by: Reckitt Benckiser LLC
Parsippany, NJ 07054-0224
Made in Canada

PRINCIPAL DISPLAY PANEL - 44 mL Bottle Carton

NDC: 63824-861-15

SCALPICIN®

2 in 1

Salicylic acid 3% Anti-dandruff Liquid

2 IN 1

Relieves
Scalp Itch

Controls
Dandruff

1.5 FL OZ (44 mL)

PRINCIPAL DISPLAY PANEL - 44 mL Bottle Carton
SCALPICIN   2 IN 1
salicylic acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 63824-861
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ) Salicylic Acid3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
water (UNII: 059QF0KO0R)  
propylene glycol (UNII: 6DC9Q167V3)  
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 63824-861-151 in 1 CARTON10/01/201211/20/2019
144 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart358H10/01/201211/20/2019
Labeler - RB Health (US) LLC (081049410)

Revised: 11/2019
Document Id: b62f1c3b-2fef-4f60-be37-49e55089419c
Set id: c072181f-827e-4e55-93e6-74929eabdbd1
Version: 3
Effective Time: 20191121
 
RB Health (US) LLC