LAVADERM AFTER SUN FOR PAIN AND ITCHING- menthol spray 
Young Living Essential Oils, LC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Lavaderm After Sun

Active ingredient

Menthol 0.5%

Purpose

Topical analgesic

Uses

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

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

Box

Label

LAVADERM AFTER SUN  FOR PAIN AND ITCHING
menthol spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70631-034
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM0.005 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70631-034-251 in 1 BOX04/05/2017
157 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34804/05/2017
Labeler - Young Living Essential Oils, LC (836136630)

Revised: 1/2023
Document Id: f1d6d188-81a7-54c0-e053-2995a90a8f1f
Set id: 4c6e4fd7-3306-2936-e054-00144ff8d46c
Version: 3
Effective Time: 20230109
 
Young Living Essential Oils, LC