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United States · US · US:47219-315_42c78db7-a105-dd6f-e063-6394a90abdca
Ultimate Pain Block
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNutra Pharma Corporation
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1147219315081 BOTTLE, DISPENSING in 1 BOX (47219-315-08) / 235 mL in 1 BOTTLE, DISPENSING
Annotations
UNII (FDA Substance ID)
ZZ4AG7L7VM
NAJA NAJA VENOM
RxCUI 1310461
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "ZZ4AG7L7VM",
"rxcui": "1310461",
"inchikey": null,
"display_name": "NAJA NAJA VENOM",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"35bc5ff5-8eb8-54cf-e063-6394a90ae3c2": {
"match": "brand_token",
"title": "ULTIMATE PHYSICAL SUNSCREEN (ZINC OXIDE) CREAM [HALEM DERMATOLOGY PLLC]",
"spl_version": "2",
"published_date": "2025-12-12"
}
},
"productid": "47219-315_42c78db7-a105-dd6f-e063-6394a90abdca",
"productndc": "47219-315",
"dosage_form": "GEL",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "NAJA NAJA VENOM",
"proprietary_name": "Ultimate Pain Block",
"active_ingred_unit": "[hp_X]/mL",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC",
"nonproprietary_name": "NAJA NAJA VENOM",
"start_marketing_date": "20251029",
"active_numerator_strength": "4"
}Access this data programmatically
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