NDC 69842-003 - Daytime and Nighttime Pain Relief
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
- 69842-003
- Package NDCs from labels
- 69842-003-20
- Manufacturer
- CVS Pharmacy, Inc. | Aurohealth LLC
- Effective date
- 2020-12-10
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Daytime and Nighttime Pain Relief - CVS Pharmacy, Inc. | Aurohealth LLC | CVS Pharmacy, Inc. | Aurohealth LLC | 2020-12-10 | Human OTC Drug Label |
DailyMed Socrata Ingredients#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Restoral | MENTHOL | Saje Natural Business Inc. | 5b6176c1-9ed9-1950-e053-2a91aa0a434e | 2026-01-13 | Warnings | L7T10EIP3A |
| Capzasin Quick Relief | CAPSAICIN AND MENTHOL | Chattem, Inc. | d6c313a3-8dc6-4231-95b6-ac9399e1c1be | 2026-01-13 | Warnings | L7T10EIP3A |
| Pain Terminator Extra Strength Pain Relief | CAFFEINE, ACETAMINOPHEN, ASPIRIN | Wildman Business Group | 8ffb02d9-92df-4d2f-a367-1c71490807fb | 2026-01-12 | Warnings | 362O9ITL9D |
| LONAZEM | MENTHOL,PETROLATUM | PEER PHARM LTD. | 91f7a741-4178-4639-9cd5-746a4b9a21bf | 2026-01-12 | Warnings | L7T10EIP3A |
| Mineral Ice Pain Relieving | MENTHOL | Crown Laboratories | 7b30076a-0af6-2f74-e053-2a91aa0ae08d | 2026-01-12 | Warnings | L7T10EIP3A |
| Sarna | PRAMOXINE HYDROCHLORIDE, MENTHOL | Crown Laboratories, Inc | 19c41e75-a654-90cf-e063-6394a90a7e97 | 2026-01-12 | Warnings | L7T10EIP3A |
| Acetaminophen and Ibuprofen | ACETAMINOPHEN AND IBUPROFEN | BIONPHARMA INC. | 4834aa7f-cb0c-ec58-e063-6394a90ae2fc | 2026-01-12 | Warnings | 362O9ITL9D |
| Itch Relief | DIPHENHYDRAMINE HCL, ZINC ACETATE | HY-VEE, INC | 48350b54-8d9a-48c4-e063-6394a90ac040 | 2026-01-12 | Warnings | TC2D6JAD40 |
| BlueStop Max | EXTERNAL ANALGESIC | Clavel Corporation | f1efb51c-5217-4cb2-e053-2a95a90a7f95 | 2026-01-12 | Warnings | L7T10EIP3A |
| Tramadol Hydrochloride and Acetaminophen | TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN | AvPAK | 244f6e5d-e1b4-ba8b-ca6f-af2d8a31d5f0 | 2026-01-12 | Warnings, Adverse reactions | 362O9ITL9D |
| OXYCODONE AND ACETAMINOPHEN | OXYCODONE AND ACETAMINOPHEN | KVK-Tech, Inc. | 9986aa04-c976-4654-8ad7-b97d2eecea93 | 2026-01-12 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| Acetaminophen | ACETAMINOPHEN | PD-Rx Pharmaceuticals, Inc. | 64696f65-415e-4ce1-a5b3-70662fbcb002 | 2026-01-12 | Warnings | 362O9ITL9D |
| Extra Strength Balm | CAPSICUM AND MENTHOL | Saje Natural Business Inc | f516e416-446b-8f21-e053-2a95a90afd88 | 2026-01-12 | Warnings | L7T10EIP3A |
| Pain Release | MENTHOL | Saje Natural Business Inc. | 3df0e56a-7651-42dc-8ed8-f68836a63c61 | 2026-01-12 | Warnings | L7T10EIP3A |
| Trauma Less | MENTHOL | Saje Natural Business Inc. | 650cba4c-6aba-48c3-9c41-841f19905548 | 2026-01-12 | Warnings | L7T10EIP3A |
| Chest Comfort | MENTHOL | Saje Natural Business Inc. | 8a3db169-6dd7-4dfd-8360-90315288f21b | 2026-01-12 | Warnings | L7T10EIP3A |
| Allergy Relief | DIPHENHYDRAMINE HCL | H E B | c9e977b6-fba6-49ea-9d80-b43b0842bbe1 | 2026-01-12 | Warnings | TC2D6JAD40 |
| Tension Headache | ACETAMINOPHEN, CAFFEINE | Cardinal Health 110, LLC. DBA Leader | 96684e3f-a13e-49c3-b437-d2627e528a2d | 2026-01-12 | Warnings | 362O9ITL9D |
| Childrens Allergy Relief | DIPHENHYDRAMINE HCL | CVS PHARMACY | 3f44cff6-240a-4a8d-aaa1-0da75a31a47b | 2026-01-12 | Warnings | TC2D6JAD40 |
| Sinu-Phen Plus Sinus Pain and Pressure | ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE | Wildman Business Group | c66e0b52-5531-4a84-ae90-8a26d27df1ec | 2026-01-12 | Warnings | 362O9ITL9D |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.