Lavaderm After Sun

Manufacturer
Twincraft inc.
Effective date
2024-09-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:54:41

Label at a glance#

ProductLavaderm After Sun For Pain and Itching
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure9 sections

Indications and uses

For the temporary relief of pain and itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites, and minor skin irritations

Dosage and administration

Shake Well Adults and children 2 years of age and older : apply to affected area not more than 3 to 4 times daily. Children under 2 years of age : ask a doctor

Storage and handling

store at controlled room temperature (68° to 77°F)

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 0.5%

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Uses

INDICATIONS & USAGE SECTION

  • For the temporary relief of pain and itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites, and minor skin irritations

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • symptoms last more than 7 days or clear up and occur again within a few days

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children to avoid accidental ingestion. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Shake Well

Adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: ask a doctor

Other information

STORAGE AND HANDLING SECTION

  • store at controlled room temperature (68° to 77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, olive oil, glycerin, safflower oil, sunflower oil, jojoba oil, polyglyceryl-10 pentastearate, glyceryl monocaprylate, helianthus annuus seed wax, European elderberry, xanthan gum, docosanol, sodium stearoyl lactylate, lavender oil, aloe vera leaf, glyceryl monoundecylenate, phytate sodium, picea mariana leaf oil, helichrysum italicum flower oil, citric add

Questions or comments?

OTC - QUESTIONS SECTION

call 1-800-371-3515

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FOR PAIN & ITCH

SOOTHES & COOLS SKIN

IMMEDIATE RELIEF

BoxBox

LabelLabel

Products#

Every source-derived product name is available through these pages.

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64412-200164412-2001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Source Document#

Source XML

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
226a324b-e4f6-ff03-e063-6294a90a69e5226a2b0c-0831-36e9-e063-6394a90a5c082024-09-18WarningsExact identifier
spl id: 226a324b-e4f6-ff03-e063-6294a90a69e5
spl set id: 226a2b0c-0831-36e9-e063-6394a90a5c08

Reported adverse events (FAERS/openFDA)#

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