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Select Brand Anti-Itch

Medically reviewed by Drugs.com. Last updated on Jan 2, 2020.

Dosage form: cream
Ingredients: PRAMOXINE HYDROCHLORIDE .1g in 10g, MENTHOL, UNSPECIFIED FORM .1g in 10g
Labeler: Select Brand
NDC Code: 15127-721

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Select Brand Anti-Itch

Drug Facts

Active ingredients

Menthol 1%

Pramoxine hydrochloride 1%

Purpose

Topical analgesic

Uses

for temporary relief of pain and itching due to:

  • minor burns
  • sunburn
  • minor cuts
  • scrapes
  • insect bites
  • minor skin irritations
  • minor rashes due to poison ivy, poison oak, or poison sumac

Warnings

For external use only

When using this product

do not get into eyes

Stop use and ask a doctor if
  • condition gets worse
  • symptoms last more than 7 days or clear up and occur again within a few days

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

adults and children 2 years and older: apply to affected area not more than 3 or 4 times daily

children under 2 years: consult a doctor

Other Information
  • store at controlled room temperature

Inactive ingredients

aloe barbadensis (aloe vera) leaf juice, diazolidinyl urea, edetate disodium, eucalyptus oil, methylparaben, methyl salicylate, mineral oil, PPG-1 trideceth-6, propylene glycol, propylparaben, purified water, sodium acrylates copolymer, steareth-21, stearyl alcohol, tocopheryl acetate, trolamine, white petrolatum

PRINCIPAL DISPLAY PANEL

Select Brand Medicated Anti-Itch Cream

Maximum Relief

Topical Analgesic

Net wt 1 oz (28.3 g)

SELECT BRAND ANTI-ITCH 
menthol and pramoxine hydrochloride cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:15127-721
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PRAMOXINE HYDROCHLORIDE (PRAMOXINE) PRAMOXINE HYDROCHLORIDE.1 g  in 10 g
MENTHOL, UNSPECIFIED FORM (MENTHOL, UNSPECIFIED FORM) MENTHOL, UNSPECIFIED FORM.1 g  in 10 g
Inactive Ingredients
Ingredient NameStrength
PROPYLPARABEN 
WATER 
METHYL SALICYLATE 
SODIUM ACRYLATE 
EDETATE DISODIUM 
METHYLPARABEN 
PPG-1 TRIDECETH-6 
STEARYL ALCOHOL 
ALOE VERA LEAF 
MINERAL OIL 
.ALPHA.-TOCOPHEROL ACETATE 
EUCALYPTUS OIL 
DIAZOLIDINYL UREA 
TROLAMINE 
PROPYLENE GLYCOL 
PETROLATUM 
Packaging
#Item CodePackage Description
1NDC:15127-721-011 TUBE in 1 CARTON
128.3 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34810/03/2012
Labeler - Select Brand (043562370)
Registrant - Weeks & Leo Co., Inc. (005290028)
Establishment
NameAddressID/FEIOperations
Weeks & Leo Co., Inc.005290028label(15127-721), manufacture(15127-721), pack(15127-721)

 
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