hemorrhoidal

Product NDC: 59779-279
11-digit product format: 597790279
Labeler code: 59779
Product ID: 59779-279_1bbf4492-a848-4bac-a1ea-f1ed628606e3
Type: HUMAN OTC DRUG
Nonproprietary name: cocoa butter, phenylephrine HCl
Dosage form: SUPPOSITORY
Route: RECTAL
Labeler: CVS Pharmacy
Application: M015
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2014-09-11
Substance: COCOA BUTTER; PHENYLEPHRINE HYDROCHLORIDE
Active strength: 2211; 6.5 mg/1; mg/1
Pharmacologic classes: Adrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC]
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product: Yes
Brand name base: hemorrhoidal
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
COCOA BUTTER	2211 mg/1
PHENYLEPHRINE HYDROCHLORIDE	6.5 mg/1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
59779-279-53	hemorrhoidal	12 in 1 CARTON	SUPPOSITORY	12	5
59779-279-53	hemorrhoidal	1 in 1 BLISTER PACK	SUPPOSITORY	1	5
59779-279-62	hemorrhoidal	24 in 1 CARTON	SUPPOSITORY	24	5
59779-279-62	hemorrhoidal	1 in 1 BLISTER PACK	SUPPOSITORY	1	5

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
59779-279-53	EA - Each	59779-279	03425aba-38c2-4716-bd47-f44647468f7a	1	2018-03-08

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
COCOA BUTTER	ACTIVE INGREDIENT	512OYT1CRR	HEMORRHOIDAL (COCOA BUTTER, PHENYLEPHRINE HCL) SUPPOSITORY [CVS PHARMACY]	2
PHENYLEPHRINE HYDROCHLORIDE	ACTIVE INGREDIENT	04JA59TNSJ	HEMORRHOIDAL (COCOA BUTTER, PHENYLEPHRINE HCL) SUPPOSITORY [CVS PHARMACY]	2
COCOA BUTTER	ACTIVE MOIETY	512OYT1CRR	HEMORRHOIDAL (COCOA BUTTER, PHENYLEPHRINE HCL) SUPPOSITORY [CVS PHARMACY]	2
PHENYLEPHRINE	ACTIVE MOIETY	1WS297W6MV	HEMORRHOIDAL (COCOA BUTTER, PHENYLEPHRINE HCL) SUPPOSITORY [CVS PHARMACY]	2
METHYLPARABEN	INACTIVE INGREDIENT	A2I8C7HI9T	HEMORRHOIDAL (COCOA BUTTER, PHENYLEPHRINE HCL) SUPPOSITORY [CVS PHARMACY]	2
PROPYLPARABEN	INACTIVE INGREDIENT	Z8IX2SC1OH	HEMORRHOIDAL (COCOA BUTTER, PHENYLEPHRINE HCL) SUPPOSITORY [CVS PHARMACY]	2
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	HEMORRHOIDAL (COCOA BUTTER, PHENYLEPHRINE HCL) SUPPOSITORY [CVS PHARMACY]	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59779-279	HEMORRHOIDAL (COCOA BUTTER, PHENYLEPHRINE HCL) SUPPOSITORY [CVS PHARMACY]	5	Current NDC, Legacy NDC, 4 package rows	20241102_e8a8431b-7851-4da0-a4fa-e242cf3daf2e.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 21 of 22 · 438 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Mayinglong Hemorrhoidal	PETROLATUM, ZINC OXIDE	Mayinglong Pharmaceutical Group Co., Ltd.	b14192ea-1bf7-da6a-e053-2a95a90a5b5e	2023-12-08	Warnings	Exact identifier application number: M015
Hemorrhoidal cooling gel	PHENYLEPHRINE HCL, WITCH HAZEL	WALGREENS	03bbe258-e00d-13cc-e063-6394a90ae345	2023-12-05	Warnings	Exact identifier application number: M015
Hemorrhoidal Pain Relief	MINERAL OIL, PETROLATUM, PHENYLEPHRINE HCL	WALGREENS	03bc5c1a-d493-5082-e063-6394a90ae87b	2023-12-05	Warnings	Exact identifier application number: M015
Bloop Hemorrhoid Relief Topical	GLYCERIN, PETROLATUM, PHENYLEPHRINE HCL, PRAMOXINE HCL	Three Nations Corp	0b6419e3-f1c7-bdfe-e063-6294a90a5d92	2023-11-30	Warnings	Exact identifier application number: M015
Bloop Fissure Healing Anorectal Topical	LIDOCAINE	Three Nations Corp	0b645092-ebc4-e4bb-e063-6294a90ad4cf	2023-11-30	Warnings	Exact identifier application number: M015
SIMPLY VITAL HEMORRHOID and ANORECTAL RELIEF	LIDOCAINE	ALPHA PLANTS INC	79fa4b89-382f-45fa-a792-90a9fe5bf573	2023-11-11	Warnings	Exact identifier application number: M015
BODY ACTION PRODUCTS Prolong Lubricating	BENZOCAINE	PRODUCT MAX GROUP INC	3bef5915-1c98-4011-baa9-ad0bbef200c2	2023-11-10	Warnings	Exact identifier application number: M015
BODY ACTION PRODUCTS Butt Eze Benzocaine	BENZOCAINE	PRODUCT MAX GROUP INC	ba75b129-7939-4373-91f5-1772976e6d61	2023-11-10	Warnings	Exact identifier application number: M015
Uber Numb Topical Anesthetic	LIDOCAINE HYDROCHLORIDE	UberScientific, LLC	441c802f-a363-1530-e054-00144ff88e88	2023-11-10	Warnings	Exact identifier application number: M015
Uber Numb Topical Anesthetic	LIDOCAINE HYDROCHLORIDE	UberScientific, LLC	4939a547-c94b-3350-e054-00144ff88e88	2023-11-10	Warnings	Exact identifier application number: M015
DR REAL NUMB Topical Anorectal	LIDOCAINE	FUZZYLULU LLC	378d8edc-2120-416d-854c-8881c2950efe	2023-11-09	Warnings	Exact identifier application number: M015
The Pharma C Company Medicated Foam with Witch Hazel	WITCH HAZEL	Kleen Test Products Corporation	1a1fbe83-be45-4654-a7bb-e934e1ccd0c6	2023-11-09	Warnings	Exact identifier application number: M015
The Pharma-C Company Medicated Hemorrhoidal Pads	WITCH HAZEL	Kleen Test Products Corporation	357703ab-4e7a-41f6-9ecf-aa98acc2d92e	2023-11-09	Warnings	Exact identifier application number: M015
DOCTORS TOUCH Erase The Pain Lidocaine	LIDOCAINE HYDROCHLORIDE	DOCTOR'S CHOICE MEDICAL, LLC	3dc9947b-8196-4a38-97b4-c2340ee77e0f	2023-11-06	Warnings	Exact identifier application number: M015
SCALAR Pain Relief Cream	MENTHOL	Miracle Balance, LLC	52a13cfe-3f46-45f8-a5af-ce07ea5758e3	2023-11-06	Warnings	Exact identifier application number: M015
SIMPLE PROMISE Simple H Hemorrhoid Relief Cream	PHENYLEPHRINE HYDROCHLORIDE, PRAMOXINE HYDROCHLORIDE	SIMPLE PROMISE PTE LTD	f6622caa-3b31-9b07-e053-2a95a90a8a51	2023-11-06	Warnings	Exact identifier application number: M015
WAXUP Numbing	LIDOCAINE HYDROCHLORIDE	CONSTRUSOLUTION, LLC	4f1645ab-1b19-4d69-99c3-9ea275b01a87	2023-11-06	Warnings	Exact identifier application number: M015
SECONDARY NUMB Lidocaine Phenylephrine Gel	LIDOCAINE, PHENYLEPHRINE HYDROCHLORIDE	LALANI Rx Consulting, Inc.	0f13f7b5-e3b1-451e-a6d6-e7e15bd04443	2023-11-06	Warnings	Exact identifier application number: M015
Brazzers Anal Desensitizing	LIDOCAINE	Metro Media Ent	ceacd80c-0dd6-4e21-97da-56da877b1c90	2023-11-06	Warnings	Exact identifier application number: M015
NUMB PLUS Maximum Strength Anorectal	LIDOCAINE	SEENEXT VENTURE LTD	a7c37b2a-b647-43d7-b43b-87bbece35430	2023-11-05	Warnings	Exact identifier application number: M015

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
512OYT1CRR	COCOA BUTTER	8002-31-1	COCOA BUTTER
04JA59TNSJ	PHENYLEPHRINE HYDROCHLORIDE	61-76-7	PHENYLEPHRINE HYDROCHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1438497	cocoa butter 88.4 % / phenylephrine HCl 0.25 % Rectal Suppository	PSN	e8a8431b-7851-4da0-a4fa-e242cf3daf2e	5
1438497	cocoa butter 0.884 MG/MG / phenylephrine hydrochloride 0.0025 MG/MG Rectal Suppository	SCD	e8a8431b-7851-4da0-a4fa-e242cf3daf2e	5
1438497	cocoa butter 88.4 % / phenylephrine HCl 0.25 % Rectal Suppository	SY	e8a8431b-7851-4da0-a4fa-e242cf3daf2e	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
59779-279-53	59779027953	12 BLISTER PACK in 1 CARTON (59779-279-53) / 1 SUPPOSITORY in 1 BLISTER PACK	12 blister pack	2014-09-11	0000-00-00	No	No	Current
59779-279-62	59779027962	24 BLISTER PACK in 1 CARTON (59779-279-62) / 1 SUPPOSITORY in 1 BLISTER PACK	24 blister pack	2014-09-11	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
CVS Pharmacy, Inc. Hemorrhoidal Suppositories Drug Facts	CVS Pharmacy	2026-10-01	HUMAN OTC DRUG LABEL	6