Lavaderm After Sun by Twincraft inc. Lavaderm After Sun

Lavaderm After Sun by

Drug Labeling and Warnings

Lavaderm After Sun by is a Otc medication manufactured, distributed, or labeled by Twincraft inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

LAVADERM AFTER SUN FOR PAIN AND ITCHING- menthol spray 
Twincraft inc.

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Lavaderm After Sun

Active ingredient

Menthol 0.5%

Purpose

Topical analgesic

Uses

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

Warnings

For external use only

When using this product

• avoid contact with 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

Keep out of reach of children.

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

Directions

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

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

Inactive ingredients

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?

call 1-800-371-3515

Principal Display Panel

FOR PAIN & ITCH

SOOTHES & COOLS SKIN

IMMEDIATE RELIEF

LAVADERM AFTER SUN  FOR PAIN AND ITCHING
menthol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64412-2001
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	0.005 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
DOCOSANOL (UNII: 9G1OE216XY)
XANTHAN GUM (UNII: TTV12P4NEE)
PICEA MARIANA LEAF OIL (UNII: Q1J49L1A5O)
GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)
WATER (UNII: 059QF0KO0R)
OLIVE OIL (UNII: 6UYK2W1W1E)
GLYCERIN (UNII: PDC6A3C0OX)
HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV)
SAFFLOWER OIL (UNII: 65UEH262IS)
SUNFLOWER OIL (UNII: 3W1JG795YI)
JOJOBA OIL (UNII: 724GKU717M)
POLYGLYCERYL-10 PENTASTEARATE (UNII: PMX5872701)
EUROPEAN ELDERBERRY (UNII: BQY1UBX046)
SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)
LAVENDER OIL (UNII: ZBP1YXW0H8)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERYL MONOUNDECYLENATE (UNII: IK8A76Q5G8)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
HELICHRYSUM ITALICUM FLOWER OIL (UNII: O97ZV7726K)
PHYTATE SODIUM (UNII: 88496G1ERL)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64412-2001-1	1 in 1 BOX	04/05/2017
1		57 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	04/05/2017

Labeler - Twincraft inc. (093248870)

Revised: 9/2024

Document Id: 226a324b-e4f6-ff03-e063-6294a90a69e5

34390-5

Set id: 226a2b0c-0831-36e9-e063-6394a90a5c08

Version: 1

Effective Time: 20240918