RevitaDERM Wound Care

Product NDC: 63347-120
11-digit product format: 633470120
Labeler code: 63347
Product ID: 63347-120_69b73949-a7e7-4e85-911e-ae688d658bbf
Type: HUMAN OTC DRUG
Nonproprietary name: BENZALKONIUM CHLORIDE
Dosage form: GEL
Route: TOPICAL
Labeler: Blaine Labs Inc.
Application: M003
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2012-05-24
Substance: BENZALKONIUM CHLORIDE
Active strength: 170 mg/89mL
NDC exclude flag: No
Listing certified through: 2026-12-31
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: RevitaDERM Wound Care
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BENZALKONIUM CHLORIDE	170 mg/89mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
F5UM2KM3W7	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1049228	Internal RxNorm lookup
1310820	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
9254dada-4e32-43a0-892b-c488d68e23e7	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63347-120-01	2022-02-18	C162847	48780-1	d6a99b39-8612-a426-e053-dadaa90af4c2	9254dada-4e32-43a0-892b-c488d68e23e7
63347-120-01	2022-01-28	C162847	48780-1	d6a99b39-8612-a426-e053-dadaa90af4c2	9254dada-4e32-43a0-892b-c488d68e23e7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63347-120-01	RevitaDERM Wound Care	89 mL in 1 TUBE	GEL	89		4

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
63347-120-01	ML - Milliliter	63347-120	19e73614-c65a-4b43-818e-92123695d054	1	2013-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
BENZALKONIUM CHLORIDE	ACTIVE INGREDIENT	F5UM2KM3W7	REVITADERM WOUND CARE (BENZALKONIUM CHLORIDE) GEL [BLAINE LABS INC.]	1
BENZALKONIUM	ACTIVE MOIETY	7N6JUD5X6Y	REVITADERM WOUND CARE (BENZALKONIUM CHLORIDE) GEL [BLAINE LABS INC.]	1
ALOE VERA LEAF	INACTIVE INGREDIENT	ZY81Z83H0X	REVITADERM WOUND CARE (BENZALKONIUM CHLORIDE) GEL [BLAINE LABS INC.]	1
BUTYLPARABEN	INACTIVE INGREDIENT	3QPI1U3FV8	REVITADERM WOUND CARE (BENZALKONIUM CHLORIDE) GEL [BLAINE LABS INC.]	1
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)	INACTIVE INGREDIENT	59TL3WG5CO	REVITADERM WOUND CARE (BENZALKONIUM CHLORIDE) GEL [BLAINE LABS INC.]	1
ETHYLPARABEN	INACTIVE INGREDIENT	14255EXE39	REVITADERM WOUND CARE (BENZALKONIUM CHLORIDE) GEL [BLAINE LABS INC.]	1
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	REVITADERM WOUND CARE (BENZALKONIUM CHLORIDE) GEL [BLAINE LABS INC.]	1
HYALURONIC ACID	INACTIVE INGREDIENT	S270N0TRQY	REVITADERM WOUND CARE (BENZALKONIUM CHLORIDE) GEL [BLAINE LABS INC.]	1
HYDROLYZED ELASTIN, BOVINE, ALKALINE (1000 MW)	INACTIVE INGREDIENT	ZR28QKN0WT	REVITADERM WOUND CARE (BENZALKONIUM CHLORIDE) GEL [BLAINE LABS INC.]	1
ISOBUTYLPARABEN	INACTIVE INGREDIENT	0QQJ25X58G	REVITADERM WOUND CARE (BENZALKONIUM CHLORIDE) GEL [BLAINE LABS INC.]	1
METHYLPARABEN	INACTIVE INGREDIENT	A2I8C7HI9T	REVITADERM WOUND CARE (BENZALKONIUM CHLORIDE) GEL [BLAINE LABS INC.]	1
PHENOXYETHANOL	INACTIVE INGREDIENT	HIE492ZZ3T	REVITADERM WOUND CARE (BENZALKONIUM CHLORIDE) GEL [BLAINE LABS INC.]	1
PROPYLPARABEN	INACTIVE INGREDIENT	Z8IX2SC1OH	REVITADERM WOUND CARE (BENZALKONIUM CHLORIDE) GEL [BLAINE LABS INC.]	1
TROLAMINE	INACTIVE INGREDIENT	9O3K93S3TK	REVITADERM WOUND CARE (BENZALKONIUM CHLORIDE) GEL [BLAINE LABS INC.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63347-120	REVITADERM WOUND CARE (BENZALKONIUM CHLORIDE) GEL [BLAINE LABS INC.]	4	Current NDC, Legacy NDC, 1 package rows	20231222_9254dada-4e32-43a0-892b-c488d68e23e7.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 2 of 115 · 2,286 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Walmart	ISOPROPYL ALCOHOL	Walmart, Inc.	2eff98ba-5736-b07e-e063-6394a90aeea9	2026-09-04	Warnings	Exact identifier application number: M003
Walgreen Alcohol	ISOPROPYL ALCOHOL	Walgreens Company	deeae1ea-3d81-4260-95be-c4f328e3fdef	2026-09-04	Warnings	Exact identifier application number: M003
Dollar General	ISOPROPYL ALCOHOL	Dollar General Corporation	00b2ef34-42d9-523c-e063-6294a90a753d	2026-09-03	Warnings	Exact identifier application number: M003
Signature Select Alcohol Prep Pads	ISOPROPYL ALCOHOL	Better Living Brands LLC	31ce72e3-03a3-1608-e063-6394a90ad850	2026-09-03	Warnings	Exact identifier application number: M003
SurviveX Sting Relief	STING RELIEF WIPE	Changzhou Maokang Medical Products Co., Ltd.	5a83b1f1-c8dc-cf07-e063-6394a90a20ca	2026-09-03	Warnings	Exact identifier application number: M003
Benzethonium chloride Plus Dyclonine hydrochloride	LIQUID BANDAGE	Kroger Co.	fe604470-917f-4cbd-a1e6-ac1dc7c57ff6	2026-09-02	Warnings	Exact identifier application number: M003
Alcohol	ISOPROPYL ALCOHOL	Rite Aid Corporation	5104f9ab-0b28-449f-a55a-5438713a24df	2026-09-02	Warnings	Exact identifier application number: M003
Hydrogen Peroxide	HYDROGEN PEROXIDE	UpLift Brands, LLC	5a81b635-d188-0b29-e063-6294a90a1e4b	2026-09-02	Warnings, Adverse reactions	Exact identifier application number: M003
Hydrogen Peroxide	HYDROGEN PEROXIDE	CVS Pharmacy, Inc.	7f518646-c8fe-499a-b5e4-8e5a5a90e01d	2026-09-02	Warnings, Adverse reactions	Exact identifier application number: M003
Alcohol	ISOPROPYL ALCOHOL	The Kroger Company	6551187f-5cde-4149-931f-b057bd760750	2026-09-02	Warnings	Exact identifier application number: M003
Unscented NasalGuard Antiseptic Topical	BENZALKONIUM CHLORIDE	TRUTEK CORP.	eb036e11-a28c-fdc0-e053-2a95a90a9cdb	2026-09-02	Warnings	Exact identifier application number: M003
Harris Teeter	ISOPROPYL ALCOHOL	Harris Teeter, LLC	d2bb20bd-ec83-8d80-e053-2a95a90a2bba	2026-09-02	Warnings	Exact identifier application number: M003
School Health	ISOPROPYL ALCOHOL	School Health Corporation	db5d0b22-f2d7-23e5-e053-2a95a90aeb51	2026-09-02	Warnings	Exact identifier application number: M003
Alcohol Prep Pads	ISOPROPYL ALCOHOL	Topco Associates	2642298f-607e-fdca-e063-6394a90a69d9	2026-09-02	Warnings	Exact identifier application number: M003
HUSTLE BUTTER NUMBING	LIDOCAINE HCL, BENZALKONIUM CHLORIDE	H.B.D. DIST. INC.	5b4d0390-dac6-4a71-9fdc-5c31543e7c5a	2026-09-02	Warnings	Exact identifier application number: M003
NasalGuard Antiseptic Topical Cool Menthol	BENZALKONIUM CHLORIDE	TRUTEK CORP.	e9fd3ef8-78ff-6c9f-e053-2a95a90a21a8	2026-09-01	Warnings	Exact identifier application number: M003
Maximum Strength Betadine Clear	BENZALKONIUM CL AND PRAMOXINE HCL	Atlantis Consumer Healthcare, Inc.	31b94a76-1536-47c0-ab03-e487c2625c58	2026-08-31	Warnings	Exact identifier application number: M003
Biopure Antibacterial Hand Wipe	ANTIBACTERIAL HAND WIPE	Fujian Yifa Healthcare Products Co., Ltd.	5a28101f-ea8e-6071-e063-6294a90aad91	2026-08-31	Warnings	Exact identifier application number: M003
Biopure Antibacterial Hand Wipe	ANTIBACTERIAL HAND WIPE	Fujian Yifa Healthcare Products Co., Ltd.	5a3e62ce-52dc-121b-e063-6294a90a898f	2026-08-31	Warnings	Exact identifier application number: M003
Biopure Antibacterial Hand Wipe	ANTIBACTERIAL HAND WIPE	Fujian Yifa Healthcare Products Co., Ltd.	5a49db18-c270-6f46-e063-6294a90afb5d	2026-08-31	Warnings	Exact identifier application number: M003

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
F5UM2KM3W7	BENZALKONIUM CHLORIDE	8001-54-5	BENZALKONIUM CHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1049228	benzalkonium chloride 0.1 % Topical Gel	PSN	9254dada-4e32-43a0-892b-c488d68e23e7	4
1310820	RevitaDERM Wound Care 0.1 % Topical Gel	PSN	9254dada-4e32-43a0-892b-c488d68e23e7	4
1310820	benzalkonium chloride 0.001 MG/MG Topical Gel [RevitaDERM Wound Care]	SBD	9254dada-4e32-43a0-892b-c488d68e23e7	4
1049228	benzalkonium chloride 0.001 MG/MG Topical Gel	SCD	9254dada-4e32-43a0-892b-c488d68e23e7	4
1049228	benzalkonium chloride 0.1 % Topical Gel	SY	9254dada-4e32-43a0-892b-c488d68e23e7	4
1310820	RevitaDERM Wound Care 0.001 MG/MG Topical Gel	SY	9254dada-4e32-43a0-892b-c488d68e23e7	4
1310820	RevitaDERM Wound Care 0.1 % Topical Gel	SY	9254dada-4e32-43a0-892b-c488d68e23e7	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63347-120-01	63347012001	89 mL in 1 TUBE (63347-120-01)	89 ml	2012-05-24	0000-00-00	No	No	Current