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United States · US · US:61010-6103_10dfe53b-4cdd-c203-e063-6294a90af360

Sunscreen

UNIISPLATC D02BA

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerSafetec of America, Inc.
CountryUS (United States)
ATC codeD02BA
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 2

  • ndc11
    6101061031
    25 PACKET in 1 BOX (61010-6103-1) / 3.5 g in 1 PACKET (61010-6103-0)
  • ndc11
    6101061033
    25 PACKET in 1 BOX (61010-6103-3) / 2 g in 1 PACKET (61010-6103-2)

Annotations

UNII (FDA Substance ID)
V06SV4M95S
HOMOSALATE
RxCUI 91326
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "V06SV4M95S",
    "rxcui": "91326",
    "inchikey": "WSSJONWNBBTCMG-UHFFFAOYSA-N",
    "display_name": "HOMOSALATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "1cb7fbca-0874-ae53-e063-6294a90ab42a": {
      "match": "brand_token",
      "title": "SUNSCREEN FOR BABY SPF50PLUS (OCTOCRYLENE,ETHYLHEXYL METHOXYCINNAMATE,TITANIUM DIOXIDE,ETHYLHEXYL SALICYLATE) LOTION [GUANGZHOU SENMAI BIOTECHNOLOGY CO., LTD.]",
      "spl_version": "7",
      "published_date": "2026-04-03"
    }
  },
  "productid": "61010-6103_10dfe53b-4cdd-c203-e063-6294a90af360",
  "productndc": "61010-6103",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE",
  "proprietary_name": "Sunscreen",
  "active_ingred_unit": "mg/g; mg/g; mg/g; mg/g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Homosalate, Octinoxate, Octisalate, Oxybenzone",
  "start_marketing_date": "20070313",
  "active_numerator_strength": "6; 7.5; 5; 5"
}

Related drugs

Other records sharing ATC code D02BA.

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