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United States · US · US:68479-020_bf9d0db0-b478-475f-aeb0-9a8ddd643ac2
Powerbright Moisturizer SPF 50
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDermalogica, LLC.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc11684790200112 mL in 1 TUBE (68479-020-01)
- ndc1168479020021 BOTTLE in 1 CARTON (68479-020-02) / 50 mL in 1 BOTTLE
- ndc1168479020057 mL in 1 TUBE (68479-020-05)
- ndc1168479020062 mL in 1 POUCH (68479-020-06)
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": {
"02c731ee-c5cb-4158-9b1f-e826593c3526": {
"match": "brand_token",
"title": "POWERBRIGHT MOISTURIZER SPF 50 (OCTOCRYLENE, HOMOSALATE, AVOBENZONE, AND OCTISALATE) LOTION [DERMALOGICA, LLC.]",
"spl_version": "2",
"published_date": "2025-01-01"
}
},
"productid": "68479-020_bf9d0db0-b478-475f-aeb0-9a8ddd643ac2",
"productndc": "68479-020",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE",
"proprietary_name": "Powerbright Moisturizer SPF 50",
"active_ingred_unit": "mg/mL; mg/mL; mg/mL; mg/mL",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Octocrylene, Homosalate, Avobenzone, and Octisalate",
"start_marketing_date": "20210304",
"active_numerator_strength": "30; 50; 30; 80"
}Access this data programmatically
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