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Rx Act Hemorrhoidal - 37808-400-16 - (Mineral oil, Petrolatum, Phenylephrine HCl, Shark liver oil)

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Drug Information of Rx Act Hemorrhoidal

Product NDC: 37808-400
Proprietary Name: Rx Act Hemorrhoidal
Non Proprietary Name: Mineral oil, Petrolatum, Phenylephrine HCl, Shark liver oil
Active Ingredient(s): 14; 71.9; .25; 3    g/100g; g/100g; g/100g; g/100g & nbsp;   Mineral oil, Petrolatum, Phenylephrine HCl, Shark liver oil
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Rx Act Hemorrhoidal

Product NDC: 37808-400
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: part346
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19951222

Package Information of Rx Act Hemorrhoidal

Package NDC: 37808-400-16
Package Description: 1 TUBE in 1 CARTON (37808-400-16) > 57 g in 1 TUBE

NDC Information of Rx Act Hemorrhoidal

NDC Code 37808-400-16
Proprietary Name Rx Act Hemorrhoidal
Package Description 1 TUBE in 1 CARTON (37808-400-16) > 57 g in 1 TUBE
Product NDC 37808-400
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Mineral oil, Petrolatum, Phenylephrine HCl, Shark liver oil
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 19951222
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name H E B
Substance Name MINERAL OIL; PETROLATUM; PHENYLEPHRINE HYDROCHLORIDE; SHARK LIVER OIL
Strength Number 14; 71.9; .25; 3
Strength Unit g/100g; g/100g; g/100g; g/100g
Pharmaceutical Classes

Complete Information of Rx Act Hemorrhoidal


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