Care Science

Product NDC: 51142-005
11-digit product format: 511420005
Labeler code: 51142
Product ID: 51142-005_562eddbb-95bb-e64b-e063-6394a90a2ff0
Type: HUMAN OTC DRUG
Nonproprietary name: diphenhydramine hydrochloride, ibuprofen, hydrocortisone, bacitracin zinc, neomycin sulfate, polymyxin-B sulfate, lidocaine HCL, benzalkonium chloride, isopropyl alcohol, ethyl alcohol
Dosage form: KIT
Route: ORAL
Labeler: ASO LLC
Application: 505G(a)(3)
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2025-05-07
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: Care Science
Listing expiration: 2027-12-31

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 7 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
106258	Internal RxNorm lookup
204602	Internal RxNorm lookup
310965	Internal RxNorm lookup
797544	Internal RxNorm lookup
1012100	Internal RxNorm lookup
1039699	Internal RxNorm lookup
1049630	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
562f2b2c-d234-e491-e063-6294a90a705f	Available on FDA.report

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Care Science	DIPHENHYDRAMINE HYDROCHLORIDE, IBUPROFEN, HYDROCORTISONE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN-B SULFATE, LIDOCAINE HCL, BENZALKONIUM CHLORIDE, ISOPROPYL ALCOHOL, ETHYL ALCOHOL	ASO LLC	562f2b2c-d234-e491-e063-6294a90a705f	2026-07-08	Warnings	Exact identifier ndc (product): 51142-005

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
51142-005-01	51142000501	1 KIT in 1 CASE (51142-005-01) * .9 g in 1 POUCH (61010-5600-1) * .34 g in 1 POUCH (51142-445-21) * .9 g in 1 POUCH (61010-5800-1) * 2 TABLET, COATED in 1 PACKET (47682-718-99) * .0019 L in 1 PACKET (61010-2017-0) * 1 TABLET, FILM COATED in 1 PACKET (47682-167-46) * .9 g in 1 PACKET (61010-5701-3)	1 kit	2025-05-07	No	No	Current