LUCKY SUPERSOFT PREMIUM- menthol zinc oxide powder

Lucky Supersoft by

Drug Labeling and Warnings

Lucky Supersoft by is a Otc medication manufactured, distributed, or labeled by Delta Brands Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Menthol 0.15%
Zinc Oxide 1.0%

Purpose

Anti Itch

Skin Protectant

Uses

Temporarily relieves the pain and itch associated with:

• Minor Cuts
• Sunburn
• Insect Bites
• Scrapes
• Prickly Heat
• Minor Burns
• Rashes
• Minor Skin Irritations
• Dries the oozing of poison ivy, oak and sumac
  

Keep out of reach of children.

Keep out of reach of children.

Warnings

For external use only.

When using this product Do not get into eyes.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.

Do not use

Do not use on Deep or puncture wounds Animal bites Serious burns. For Powder products Do not use on Broken skin. When using this product Keep away from face and mouth to avoid breathing it.

Directions

Apply as needed, dry skin completely prior to using. Children under 2 years of age, consult a doctor.

Inactive Ingredients

Talc, Eucalyptus Oil, Methyl Salicylate, Salicylic Acid, Thymol, Camphor, Zinc Stearate

Package Label

INGREDIENTS AND APPEARANCE

LUCKY SUPERSOFT  PREMIUM
menthol zinc oxide powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 20276-979
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	0.15 g  in 100 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
TALC (UNII: 7SEV7J4R1U)
EUCALYPTUS OIL (UNII: 2R04ONI662)
METHYL SALICYLATE (UNII: LAV5U5022Y)
SALICYLIC ACID (UNII: O414PZ4LPZ)
THYMOL (UNII: 3J50XA376E)
CAMPHOR (NATURAL) (UNII: N20HL7Q941)
ZINC STEARATE (UNII: H92E6QA4FV)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 20276-979-10	283 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/25/2010

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	10/25/2010

Labeler - Delta Brands Inc (102672008)