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United States · US · US:49404-307_2d82a7ff-8d4d-02d2-e063-6394a90a2347
DR.JART EVERY SUN DAY SUN FLUID
UNIISPLATC D02BA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHave & Be Co., Ltd.
CountryUS (United States)
ATC codeD02BA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1149404307011 BOTTLE in 1 CARTON (49404-307-01) / 100 mL in 1 BOTTLE
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": {
"45b1c2c6-a45b-4a45-bec9-e5341079c0a1": {
"match": "brand_token",
"title": "DR.JART PREMIUM BEAUTY BALM LIGHT MEDIUM-MEDIUM (ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE) CREAM [HAVE & BE CO., LTD.]",
"spl_version": "5",
"published_date": "2026-01-12"
}
},
"productid": "49404-307_2d82a7ff-8d4d-02d2-e063-6394a90a2347",
"productndc": "49404-307",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE",
"proprietary_name": "DR.JART EVERY SUN DAY SUN FLUID",
"active_ingred_unit": "mg/mL; mg/mL; mg/mL; mg/mL; mg/mL",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "homosalate, octinoxate, octisalate, octocrylene, avobenzone",
"start_marketing_date": "20230811",
"active_numerator_strength": "29; 90; 68; 45; 40"
}Related drugs
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