dermalogica dynamic skin recovery spf 50

UNIISPL

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

Identification

ManufacturerDermalogica, LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 5

ndc11
6847938200
2 mL in 1 POUCH (68479-382-00)
ndc11
6847938201
12 mL in 1 TUBE (68479-382-01)
ndc11
6847938202
50 mL in 1 BOTTLE, PUMP (68479-382-02)
ndc11
6847938203
1 BOTTLE in 1 CARTON (68479-382-03) / 100 mL in 1 BOTTLE
ndc11
6847938241
118 mL in 1 TUBE (68479-382-41)

Annotations

UNII (FDA Substance ID)

G63QQF2NOX

AVOBENZONE

RxCUI 45045

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "G63QQF2NOX",
    "rxcui": "45045",
    "inchikey": "XNEFYCZVKIDDMS-UHFFFAOYSA-N",
    "display_name": "AVOBENZONE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "051b77ab-6970-48e4-bbfd-c066178ea32e": {
      "match": "brand_token",
      "title": "DERMALOGICA DYNAMIC SKIN RECOVERY SPF 50 (SUNSCREEN) LOTION [DERMALOGICA, LLC]",
      "spl_version": "3",
      "published_date": "2024-10-24"
    }
  },
  "productid": "68479-382_6c5de8bd-95aa-474a-8b4f-7e888a2edfcb",
  "productndc": "68479-382",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE",
  "proprietary_name": "dermalogica dynamic skin recovery spf 50",
  "active_ingred_unit": "g/100mL; g/100mL; g/100mL; g/100mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Sunscreen",
  "start_marketing_date": "20220117",
  "active_numerator_strength": "3; 5; 3; 7"
}

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