HERPETINO COLD SORE RELIEF TERRY NATURALLY BRAND- allantoin cream

Herpetino Cold Sore Relief Terry Naturally Brand by

Drug Labeling and Warnings

Herpetino Cold Sore Relief Terry Naturally Brand by is a Otc medication manufactured, distributed, or labeled by EuroPharma, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Allantoin 1%

Purpose

Cold sore/fever blister treatment and skin protectant

Uses

Relieves dryness and softens cold sores and fever blisters.
Softens scabs associated with cold sores and fever blisters.
Helps prevent, protect, and soothe chapped, cracked skin and lips.

Warnings

For external use only.

When using this product 

Avoid contact with eyes.

Do not use on: 

deep or puncture wounds animal bites serious burns

Stop use and ask a doctor if

Condition worsens Symptoms last more than 7 days or clear up and occur again within a few days.

Keep out of the reach of children. 

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

Directions:

Apply at first sign of cold sore or fever blister, several times daily.

Inactive ingredients:

Bisabolol (Chamomile), Dimethicone, Hexyl Laurate, Jojoba (Simmondsia Chinensis) Seed Oil, Panthenol, Polyglyceryl-4 Isostearate, Polyisobutane, Propolis Extract, Shea (Butyrospermum Parkii) Butter, Sodium Chloride, Sweet Almond (Amygdalus Dulcis) Oil, Tocopheryl Acetate, Water, Xylitol.

Package Labeling:

INGREDIENTS AND APPEARANCE

HERPETINO COLD SORE RELIEF TERRY NATURALLY BRAND 
allantoin cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67703-000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	10 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
CHAMOMILE (UNII: FGL3685T2X)
DIMETHICONE (UNII: 92RU3N3Y1O)
HEXYL LAURATE (UNII: 4CG9F9W01Q)
JOJOBA OIL (UNII: 724GKU717M)
PANTHENOL (UNII: WV9CM0O67Z)
POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
PROPOLIS WAX (UNII: 6Y8XYV2NOF)
SHEA BUTTER (UNII: K49155WL9Y)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
ALMOND OIL (UNII: 66YXD4DKO9)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)
XYLITOL (UNII: VCQ006KQ1E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67703-000-00	1 in 1 BOX	03/15/2018	10/31/2020
1		10 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	03/15/2018	10/31/2020

Labeler - EuroPharma, Inc (060446577)

Registrant - EuroPharma, Inc (060446577)