TEEVODAR- allantoin cream

Teevodar by

Drug Labeling and Warnings

Teevodar by is a Otc medication manufactured, distributed, or labeled by PEER PHARM LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Allantoin 0.5%

Purpose

Skin Protectant

Uses

Temporarily protects minor cuts scrapes burns

Warnings

• For external use only
• When using this product do not get into eyes
• Stop use and ask a doctor if 
• contition worsens 
• 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.

KEEP OUT OF REACH OF CHILDREN

Directions

• Apply as needed. 
• Children under 12 years of age: consult a doctor

Inactive Ingredients

Ceteareth-20, Cetearyl alcohol, Cetyl alcohol, ethylhexylglycerin, Hamamelis virginiana (witch hazel) leaf extract, Isopropyl myristate, Lanolin, Mineral oil, Origanum vulgare (oregano) leaf extract, Petrolatum, Phenoxyethanol, Purified water, Rosmarinus officinalis (rosemary) leaf extract, Zea mayes (corn) oil

Product label

INGREDIENTS AND APPEARANCE

TEEVODAR 
allantoin cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69435-1301
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CETYL ALCOHOL (UNII: 936JST6JCN)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
LANOLIN (UNII: 7EV65EAW6H)
MINERAL OIL (UNII: T5L8T28FGP)
OREGANO (UNII: 0E5AT8T16U)
PETROLATUM (UNII: 4T6H12BN9U)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)
ROSEMARY (UNII: IJ67X351P9)
CORN OIL (UNII: 8470G57WFM)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69435-1301-1	1 in 1 CARTON	05/15/2023
1		30 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	05/15/2023

Labeler - PEER PHARM LTD. (514678390)

Registrant - PEER PHARM LTD. (514678390)