LavaDerm AfterSun

SPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerYoung Living Essential Oils, LC.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7063106757
1 BOTTLE, SPRAY in 1 BOX (70631-067-57) / 57 g in 1 BOTTLE, SPRAY

Annotations

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "route": "TOPICAL",
  "spl_meta": {
    "4fcddcf1-36db-2f1a-e054-00144ff8d46c": {
      "match": "brand_token",
      "title": "LAVADERM AFTERSUN (MENTHOL) SPRAY [YOUNG LIVING ESSENTIAL OILS, LC.]",
      "spl_version": "4",
      "published_date": "2026-05-06"
    }
  },
  "productid": "70631-067_4f8770bb-310d-48d9-e063-6294a90afcdb",
  "productndc": "70631-067",
  "dosage_form": "SPRAY",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MENTHOL",
  "proprietary_name": "LavaDerm AfterSun",
  "active_ingred_unit": "g/100g",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Menthol",
  "start_marketing_date": "20240418",
  "active_numerator_strength": ".5"
}

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