NDC 61010-5701-3 - Walgreens

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 61010-5701
Requested NDC: 61010-5701-3
Package NDCs from labels: 61010-5701-3, 61010-5701-4, 61010-5701-5, 61010-5701-6
Manufacturer: Walgreen Co.
Effective date: 2026-07-09
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Walgreens All-Purpose First Aid Kit 150 pieces	Walgreen Co.	2026-07-09	HUMAN OTC DRUG LABEL
Care Science - ASO LLC	ASO LLC	2026-07-08	HUMAN OTC DRUG LABEL
First Aid Only First Aid-Burn - Acme United Corporation	Acme United Corporation	2024-12-18	HUMAN OTC DRUG LABEL
61010-5701, First Aid and Burn Cream	Safetec of America, Inc.	2024-02-07	HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
61010-5701-4	2024-02-07	61010-5701, First Aid and Burn Cream
61010-5701-5	2024-02-07	61010-5701, First Aid and Burn Cream
61010-5701-6	2024-02-07	61010-5701, First Aid and Burn Cream
61010-5701-4	2024-01-30	61010-5701, First Aid and Burn Cream
61010-5701-5	2024-01-30	61010-5701, First Aid and Burn Cream
61010-5701-6	2024-01-30	61010-5701, First Aid and Burn Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
61010-5701-3	First Aid and Burn	0.9 g in 1 PACKET	CREAM	0.9	5
61010-5701-4	First Aid and Burn	144 in 1 BOX	CREAM	144	5
61010-5701-5	First Aid and Burn	25 in 1 BOX	CREAM	25	5
61010-5701-6	First Aid and Burn	10 in 1 BOX	CREAM	10	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
61010-5701	FIRST AID AND BURN (BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE) CREAM [SAFETEC OF AMERICA, INC.]	5	Current NDC, Legacy NDC, 4 package rows	20240208_47cb6921-5d82-4123-a9e0-0b05d4dcb5b2.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
benzalkonium chloride	ACTIVE INGREDIENT	F5UM2KM3W7	FIRST AID AND BURN (BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE) CREAM [SAFETEC OF AMERICA, INC.]	1
lidocaine hydrochloride	ACTIVE INGREDIENT	V13007Z41A	FIRST AID AND BURN (BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE) CREAM [SAFETEC OF AMERICA, INC.]	1
benzalkonium	ACTIVE MOIETY	7N6JUD5X6Y	FIRST AID AND BURN (BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE) CREAM [SAFETEC OF AMERICA, INC.]	1
lidocaine	ACTIVE MOIETY	98PI200987	FIRST AID AND BURN (BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE) CREAM [SAFETEC OF AMERICA, INC.]	1
alcohol	INACTIVE INGREDIENT	3K9958V90M	FIRST AID AND BURN (BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE) CREAM [SAFETEC OF AMERICA, INC.]	1
aloe vera leaf	INACTIVE INGREDIENT	ZY81Z83H0X	FIRST AID AND BURN (BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE) CREAM [SAFETEC OF AMERICA, INC.]	1
methylparaben	INACTIVE INGREDIENT	A2I8C7HI9T	FIRST AID AND BURN (BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE) CREAM [SAFETEC OF AMERICA, INC.]	1
mineral oil	INACTIVE INGREDIENT	T5L8T28FGP	FIRST AID AND BURN (BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE) CREAM [SAFETEC OF AMERICA, INC.]	1
paraffin	INACTIVE INGREDIENT	I9O0E3H2ZE	FIRST AID AND BURN (BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE) CREAM [SAFETEC OF AMERICA, INC.]	1
petrolatum	INACTIVE INGREDIENT	4T6H12BN9U	FIRST AID AND BURN (BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE) CREAM [SAFETEC OF AMERICA, INC.]	1
propylparaben	INACTIVE INGREDIENT	Z8IX2SC1OH	FIRST AID AND BURN (BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE) CREAM [SAFETEC OF AMERICA, INC.]	1
water	INACTIVE INGREDIENT	059QF0KO0R	FIRST AID AND BURN (BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE) CREAM [SAFETEC OF AMERICA, INC.]	1
white wax	INACTIVE INGREDIENT	7G1J5DA97F	FIRST AID AND BURN (BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE) CREAM [SAFETEC OF AMERICA, INC.]	1

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 879 · 17,565 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
North Woods Derma Foam Hand Sanitizer	BENZALKONIUM CHLORIDE	Superior Chemical Corporation	ad51a175-2b91-fd14-e053-2995a90ad54d	2026-09-09	Warnings	Exact identifier unii: F5UM2KM3W7
MUCINEX FAST-MAX Liquid Gels Day Night Cold and Flu	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND DOXYLAMINE SUCCINATE	Reckitt Benckiser LLC	3856c1e4-814f-85c4-e063-6394a90ab8a8	2026-09-09	Warnings	Exact identifier application number: M012
Touchland Power Mist Hydrating Hand Sanitizer Cotton Candy	ALCOHOL	Church & Dwight Co., Inc.	5b107dd2-a76c-9c80-e063-6394a90aaedb	2026-09-09	Warnings	Exact identifier unii: 3K9958V90M
Pink Touchland Power Mist Hydrating Hand Sanitizer Wild Watermelon	ALCOHOL	Church & Dwight Co., Inc.	5b108f13-6474-fdbd-e063-6294a90a1a2b	2026-09-09	Warnings	Exact identifier unii: 3K9958V90M
Touchland Power Mist Hydrating Hand Sanitizer Mango Passion	ALCOHOL	Church & Dwight Co., Inc.	5b1099ae-f1e8-b79d-e063-6394a90add6f	2026-09-09	Warnings	Exact identifier unii: 3K9958V90M
Touchland Gentle Mist Hand Sanitizer Lily of The Valley	ALCOHOL	Church & Dwight Co., Inc.	5b10a3a7-1cca-2a34-e063-6294a90a3f6c	2026-09-09	Warnings	Exact identifier unii: 3K9958V90M
Alcohol Free Foaming Hand Sanitizer	BENZALKONIUM CHLORIDE	Betco Corporation, Ltd.	7e038b0a-4813-4f4b-ad66-0584d75a064f	2026-09-09	Warnings	Exact identifier unii: F5UM2KM3W7
Burn Cream	BENZALKONIUM CHLORIDE, LIDOCAINE HCI	Trifecta Pharmaceuticals USA LLC	e9a9fc7c-31da-ea3f-e053-2a95a90a0eab	2026-09-09	Warnings	Exact identifier application number: M003 rxcui: 1012100 unii: F5UM2KM3W7 unii: V13007Z41A
Ultra Blue Antibacterial Foaming Skin Cleanser	BENZALKONIUM CHLORIDE	Betco Corporation, Ltd	aa8f5b05-882d-d05a-e053-2995a90abaea	2026-09-09	Warnings	Exact identifier unii: F5UM2KM3W7
Burn Gel	LIDOCAINE HCI	Trifecta Pharmaceuticals USA LLC	e9d3e9be-1036-fad0-e053-2a95a90a6efe	2026-09-09	Warnings	Exact identifier application number: M017 unii: V13007Z41A
Touchland Glow Mist Hand Sanitizer Rosewater	ALCOHOL	Church & Dwight Co., Inc.	5a850866-bc5d-e595-e063-6394a90a335f	2026-09-09	Warnings	Exact identifier unii: 3K9958V90M
Ibuprofen	IBUPROFEN	Lidl US LLC	0ca02f8b-4413-4e7c-a67b-8c67c53e1343	2026-09-09	Warnings	Exact identifier application number: ANDA079174 rxcui: 310965 unii: WK2XYI10QM
Ibuprofen	IBUPROFEN	GOODSENSE	596a1007-08ea-00ec-e063-6394a90a5eb2	2026-09-09	Warnings	Exact identifier unii: WK2XYI10QM
Leader Artificial Tears 15 mL	POLYVINYL ALCOHOL, POVIDONE	Cardinal Health	8cccc589-3a8e-baad-e053-2a95a90ab8c7	2026-09-09	Warnings	Exact identifier unii: 532B59J990
Triple Antibiotic	BACITRACIN ZINC, NEOMYCIN SULFATE, AND POLYMYXIN B SULFATE	NuCare Pharmaceutical, Inc.	5b14499e-e45c-7c05-e063-6294a90a1cc2	2026-09-09	Warnings	Exact identifier application number: M004 rxcui: 204602 unii: 89Y4M234ES unii: 057Y626693 unii: 19371312D4
Drs. Pharmacy baby healing	PETROLATUM	OL PHARMA TECH, LLC Drs PHARMACY	5b14ffa0-9486-a7fe-e063-6394a90ab3ed	2026-09-09	Warnings	Exact identifier unii: 4T6H12BN9U
4% Lidocaine Pain Relief Patch	LIDOCAINE 4%	Guangxi Keyun E-commerce Co., Ltd.	5b197cd8-542f-38b4-e063-6294a90ad7d3	2026-09-09	Warnings	Exact identifier application number: M017
ibuprofen childrens	IBUPROFEN	Rite Aid Corporation	c6e68886-edcb-414d-9cba-0d97772ef8b6	2026-09-09	Warnings	Exact identifier unii: WK2XYI10QM
DRx Choice Long Acting Cough	DEXTROMETHORPHAN HBR	RARITAN PHARMACEUTICALS	875b40bd-7955-4048-abbf-7f43d9ea3ac5	2026-09-09	Warnings	Exact identifier application number: M012
severe cold and flu relief	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDE	Rite Aid Corporation	4b8ae971-ab57-4937-a878-72d905d7b849	2026-09-09	Warnings	Exact identifier application number: M012

Reported adverse events (FAERS/openFDA)#

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