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United States · US · US:10742-8160_2978fba5-0be6-3179-e063-6294a90a182a
Rohto Optic Glow
UNIISPLATC R01AA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerThe Mentholatum Company
CountryUS (United States)
ATC codeR01AA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1110742816011 BOTTLE, WITH APPLICATOR in 1 CARTON (10742-8160-1) / 13 mL in 1 BOTTLE, WITH APPLICATOR
Annotations
UNII (FDA Substance ID)
MZ1131787D
NAPHAZOLINE HYDROCHLORIDE
RxCUI 82054
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "MZ1131787D",
"rxcui": "82054",
"inchikey": "DJDFFEBSKJCGHC-UHFFFAOYSA-N",
"display_name": "NAPHAZOLINE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "OPHTHALMIC",
"spl_meta": {
"1b597f83-d7f1-cf93-e063-6394a90a99f7": {
"match": "brand_token",
"title": "ROHTO DUAL LIGHT RELIEF (HYPROMELLOSE, POVIDONE) LIQUID [THE MENTHOLATUM COMPANY]",
"spl_version": "3",
"published_date": "2024-12-23"
}
},
"productid": "10742-8160_2978fba5-0be6-3179-e063-6294a90a182a",
"productndc": "10742-8160",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "NAPHAZOLINE HYDROCHLORIDE; POVIDONE, UNSPECIFIED; PROPYLENE GLYCOL",
"proprietary_name": "Rohto Optic Glow",
"active_ingred_unit": "mg/mL; mg/mL; mg/mL",
"application_number": "M018",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Naphazoline hydrochloride, Povidone, Propylene glycol",
"start_marketing_date": "20210326",
"active_numerator_strength": ".3; 5; 2"
}Related drugs
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