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United States · US · US:67777-410_4bbb8bb6-6564-7aee-e063-6294a90a5903
Lanashield
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDynarex Corporation
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc11677774100324 TUBE in 1 CASE (67777-410-03) / 113 g in 1 TUBE (67777-410-04)
- ndc1167777410072 BOX in 1 CASE (67777-410-07) / 144 PACKET in 1 BOX (67777-410-06) / 5 g in 1 PACKET (67777-410-05)
- ndc11677774101236 JAR in 1 CASE (67777-410-12) / 71 g in 1 JAR (67777-410-11)
- ndc11677774101412 JAR in 1 CASE (67777-410-14) / 397 g in 1 JAR (67777-410-13)
Annotations
UNII (FDA Substance ID)
7EV65EAW6H
LANOLIN
RxCUI 6227
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "7EV65EAW6H",
"rxcui": "6227",
"inchikey": null,
"display_name": "LANOLIN",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"94b277dc-6512-4d36-8485-8ea510097428": {
"match": "brand_token",
"title": "LANASHIELD (LANOLIN) OINTMENT [DYNAREX CORPORATION]",
"spl_version": "10",
"published_date": "2026-03-02"
}
},
"productid": "67777-410_4bbb8bb6-6564-7aee-e063-6294a90a5903",
"productndc": "67777-410",
"dosage_form": "OINTMENT",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "LANOLIN",
"proprietary_name": "Lanashield",
"active_ingred_unit": "g/100g",
"application_number": "M016",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Lanolin",
"start_marketing_date": "20141012",
"active_numerator_strength": "50"
}Access this data programmatically
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