Lucky Supersoft Medicated Body

Manufacturer
Delta Brands Inc
Effective date
2022-05-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:00:24

Label at a glance#

ProductLucky Supersoft Medicated Body Triple Action
Active ingredientMENTHOL, ZINC OXIDE
Label structure12 sections

Indications and uses

temporarily relieves the pain and itch associated with: ■ minor cuts ■ sunburn ■ insect bites ■ scrapes ■ minor burns ■ minor skin irritations

Dosage and administration

■ for aduts and children 2 years and older: apply freely up to 3 or 4 times daily ■ for children under 2 years: ask a doctor ■ for best results dry skin thoroughly before applying​

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 0.15%
Zinc oxide 1.0%

Purpose

OTC - PURPOSE SECTION

Anti-itch

Skin protectant

Uses

INDICATIONS & USAGE SECTION

temporarily relieves the pain and itch associated with:

■ minor cuts ■ sunburn ■ insect bites ■ scrapes ■ minor burns ■ minor skin irritations

Warnings

WARNINGS SECTION

For external use only

Do not use on

OTC - DO NOT USE SECTION

■ broken skin ■ deep or puncture wounds ■ serious burns

When using this product

OTC - WHEN USING SECTION

■ avoid contct with eyes ■ ​keep away from face and mouth to avoid breathing powder

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ if condition worsens ■ symptoms persist for more than 7 days or clear up and occur again within a few days ■ redness, irritation, swelling or pain persists or increases

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

■ for aduts and children 2 years and older: apply freely up to 3 or 4 times daily ■ for children under 2 years: ask a doctor ■ for best results dry skin thoroughly before applying​

Other information

SPL UNCLASSIFIED SECTION

■ this product is sold by weight, not by volume ■ settling will occur during handling & shipping

Inactive ingredients

INACTIVE INGREDIENT SECTION

acacia seyal gum, eucalyptol, methyl salicylate, salicylic acid, sodium bicarbonate, thymol, tricalcium phsphate, zea mays (corn) starch, zinc stearate

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PAckage LabelPAckage Label

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
20276-98020276-980-08, 20276-980-14

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
dfff9f17-9b4a-dd76-e053-2995a90a7b40603c6f66-93e1-0484-e053-2a91aa0a075a2022-05-27WarningsExact identifier
spl id: dfff9f17-9b4a-dd76-e053-2995a90a7b40
spl set id: 603c6f66-93e1-0484-e053-2a91aa0a075a

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.