SUPER LYSINE PLUS- menthol, unspecified form ointment

Super Lysine plus by

Drug Labeling and Warnings

Super Lysine plus by is a Otc medication manufactured, distributed, or labeled by Quantum, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Menthol 0.1%

Purpose

Cold sore / fever blister treatment

Uses

Relieves tingling, itching, burning, blistering, and pain associated with cold sores/fever blisters.

Warnings

For external use only.

When using this product do not get into eyes.

Stop use and ask a doctor if

• condition worsens; or
• symptoms last more than 7 days or clear up and occur again

Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right away.

Directions

For adults and children 2 and older. Apply liberally as needed. For best results, apply every 2 hours. Wash hands before and after applying.

Other Information

• Store at room temperature and avoid excessive heat.
• Close cover tightly after each use.

Inactive Ingredients

Beeswax, Calendula Officinalis Extract, Echinacea Purpurea Extract, Gum Benzoin Tincture, Honey, Hydrastis Canadensis (Goldenseal) Leaf, Lysine, Melaleuca Alternifolia Oil, Melaleuca Cajuputi Oil, Olea Europaea (Olive) Fruit Oil, Propolis Extract, Vitamin A (Retinyl Palmitate), Vitamin D3, Vitamin E (Tocopherol), Zinc Oxide.

SPL UNCLASSIFIED SECTION

DISTRIBUTED BY: QUANTUM, INC.
PO BOX 2791, EUGENE, OR 97402

PRINCIPAL DISPLAY PANEL - 7 g Tube Carton

Quantum®
HEALTH

SuperLysine+®

Cold Sore Treatment
CUTS HEALING TIME IN HALF*

SOOTHES & MOISTURIZES
RELIEVES PAIN, BURNING, & ITCHING

LYSINE PLUS PROPOLIS, OLIVE OIL,
VITAMIN E, & 10 OTHER NUTRIENTS

Ointment

NET WT 7g / .25 OZ

INGREDIENTS AND APPEARANCE

SUPER LYSINE PLUS 
menthol, unspecified form ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70084-420
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Menthol, Unspecified Form (UNII: L7T10EIP3A) (Menthol, Unspecified Form - UNII:L7T10EIP3A)	Menthol, Unspecified Form	1 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
Calendula Officinalis Flower (UNII: P0M7O4Y7YD)
Echinacea Purpurea (UNII: QI7G114Y98)
BENZOIN RESIN (UNII: GK21SBA74R)
HONEY (UNII: Y9H1V576FH)
GOLDENSEAL (UNII: ZW3Z11D0JV)
LYSINE HYDROCHLORIDE (UNII: JNJ23Q2COM)
TEA TREE OIL (UNII: VIF565UC2G)
MELALEUCA CAJUPUTI LEAF OIL (UNII: 5O59RMR6DU)
OLIVE OIL (UNII: 6UYK2W1W1E)
PROPOLIS WAX (UNII: 6Y8XYV2NOF)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
CHOLECALCIFEROL (UNII: 1C6V77QF41)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
ZINC OXIDE (UNII: SOI2LOH54Z)
Yellow Wax (UNII: 2ZA36H0S2V)

Product Characteristics
Color	GREEN (Olive Green)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70084-420-21	1 in 1 CARTON	10/01/1984
1		21 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 70084-420-07	1 in 1 CARTON	10/01/1984
2		7 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	part341	10/01/1984

Labeler - Quantum, Inc. (044806305)