All Day Moisture

UNIISPL

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

Identification

ManufacturerWalmart Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7990331306
1 BOTTLE in 1 CARTON (79903-313-06) / 177 mL in 1 BOTTLE

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": {
    "8889af37-8345-4358-994d-7d8b847f4874": {
      "match": "brand_token",
      "title": "ALL DAY ALLERGY (CETIRIZINE HYDROCHLORIDE) TABLET, FILM COATED [HYVEE INC]",
      "spl_version": "6",
      "published_date": "2026-05-13"
    }
  },
  "productid": "79903-313_4a93acc0-1283-e13c-e063-6294a90aef09",
  "productndc": "79903-313",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "HOMOSALATE; ZINC OXIDE",
  "proprietary_name": "All Day Moisture",
  "active_ingred_unit": "mg/mL; mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Homosalate, Zinc Oxide",
  "start_marketing_date": "20250130",
  "active_numerator_strength": "50; 30"
}

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