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TACT

Medically reviewed by Drugs.com. Last updated on Aug 30, 2021.

Dosage form: cream
Ingredients: DIPHENHYDRAMINE HYDROCHLORIDE 2g in 100g, LEVOMENTHOL 1g in 100g
Labeler: Sato Pharmaceutical Inc., Ltd.
NDC Code: 49873-705

DRUG FACTS

Active ingredients  
Diphenhydramine hydrochloride 2.0%
Menthol 1.0%

Purpose   
Diphenhydramine Hydrochloride    External analgesic
l-Menthol    External analgesic

Uses
temporarily relieves pain and itching associated with
■ minor skin irritations    ■ insect bites    ■ minor cuts    ■ scrapes
■ rashes due to poison ivy    ■ sunburn        ■ minor burns

Warnings
For rectal use only

When using this product

■ avoid contact with the eyes

Stop use and ask a doctor if

■ condition worsens ■ symptoms persist for more than 7 days.

■ symptoms 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 over:  Apply to affected area not more than 3 to 4 times daily.
■ children under 2 years:  Ask a doctor.

Inactive ingredients  butylparaben, carboxyvinyl polymer, cetyl alcohol, diethanolamine, edetate disodium, light mineral oil, PEG-40 stearate, propylene glycol, propylparaben, purified water, sorbitan monostearate, white petrolatum.


tactcreamcart.jpg

TACT 
diphenhydramine hydrochloride, menthol cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49873-705
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (DIPHENHYDRAMINE) DIPHENHYDRAMINE HYDROCHLORIDE2 g  in 100 g
LEVOMENTHOL (LEVOMENTHOL) LEVOMENTHOL1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
BUTYLPARABEN 
CARBOMER HOMOPOLYMER TYPE C 
CETYL ALCOHOL 
DIETHANOLAMINE 
EDETATE SODIUM 
LIGHT MINERAL OIL 
PEG-40 STEARATE 
PROPYLENE GLYCOL 
PROPYLPARABEN 
WATER 
SORBITAN MONOSTEARATE 
PETROLATUM 
Packaging
#Item CodePackage Description
1NDC:49873-705-011 TUBE in 1 CARTON
120 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34809/09/1997
Labeler - Sato Pharmaceutical Inc., Ltd. (690575642)
Establishment
NameAddressID/FEIOperations
Sato Pharmaceutical Inc., Ltd.715699133manufacture(49873-705), label(49873-705), pack(49873-705)

 
Sato Pharmaceutical Inc., Ltd.

Further information

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