Pain Relief

Product NDC: 63868-175
11-digit product format: 638680175
Labeler code: 63868
Product ID: 63868-175_9b26e025-90a0-430c-8cef-bb8439892194
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen
Dosage form: SUSPENSION
Route: ORAL
Labeler: QUALITY CHOICE (Chain Drug Marketing Association)
Application: M013
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2015-10-31
Substance: ACETAMINOPHEN
Active strength: 160 mg/5mL
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 6 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	63868-175-26	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	63868-175-26	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	63868-175-26	`557ba5c1ecfa…`	`9c80585c8c6e…`

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: Pain Relief
Brand name suffix: Childrens
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ACETAMINOPHEN	160 mg/5mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
362O9ITL9D	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
307668	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
223ffb2b-3ee5-4118-955b-bc4fa4e8a2e6	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
75d4bef7-334c-4a95-abb5-bff9def24114	Product name	2	20260112
7dea7767-9f52-b60a-5435-33cb9cc28bae	Product name	4	20250124
6338270f-96cb-0ecb-6fbb-0a9bc78001f4	Product name	7	20250116
11939cf5-0ea7-5df5-5127-00a7ce07fd7f	Product name	5	20250115
0ca83774-3f79-b837-5d6f-c210102f3bc8	Product name	6	20250114
88300afc-e1c4-ad17-c80b-4957f1b809a5	Product name	5	20250113
4eddd6ca-259a-4c6c-a3a4-2025015ce043	Product name	7	20240611
16cde546-8deb-4df2-a072-dab5566ede95	Product name	1	20231003
20ab58de-c64a-4ec2-9210-3aa3fae2b66f	Product name	1	20230808
e2db08c6-133f-4f4f-afb4-e90a2418d6f6	Product name	1	20230320
a3631b20-02d1-41d7-8187-5e5e850b9e80	Product name	1	20230306
79e1734e-f721-4d46-978a-be382f771672	Product name	2	20230110
41b814f3-0166-1c53-c9ef-a0794c7daf9d	Product name	3	20221110
a590be26-846c-8659-a5a1-fb25907965dc	Product name	2	20221110
06cc817f-60e0-4473-8e6b-c44d11dc5af6	Product name	9	20220921
92ead9ae-674d-4eee-a492-c385d496891f	Product name	3	20220308
c6f86816-7da6-43ea-8c25-ac9758311cc5	Product name	1	20220118
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906	Product name	7	20210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206	Product name	1	20201029
103b151b-b17f-42ac-8624-3ef62f5e2975	Product name	2	20200507
b8497372-efe9-9dde-fa2d-59be9761aa64	Product name	9	20200428
20c8cafe-5cfc-44f8-a9be-a664f437f780	Product name	2	20200225
3a16d77a-e865-468a-aedf-6e58913c1c21	Product name	3	20190619
2a0c98e1-033f-4e0d-a0da-b5291ffbe880	Product name	1	20190320
00d531e4-b130-8c52-eaf9-826cbb6f15dd	Product name	3	20190205
aa0f353d-f35e-62e4-4e1f-5b563f01c659	Product name	9	20190205
22d922aa-c443-d9f3-b23c-03b03a9ad31c	Product name	7	20181220
11ed6f83-cdd2-4637-8379-b1a1d3ae3cde	Product name	1	20181101
86c45a79-b9f0-4476-a27c-6e10db098497	Product name	1	20180125
252e11b6-1a9a-4283-a242-df2c129c496d	Product name	3	20170717
377068df-225f-7318-a910-a1987cdfa361	Product name	3	20170608
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831
23475c0b-a5b5-4fec-b97f-acca901eae6a	Product name	1	20140718
105ef617-6fa4-6713-326f-72ec8a6b75a9	Product name	1	20140508
332e86c3-7875-ca6e-f934-2206d2b31996	Product name	1	20140508
3ed6b849-48b8-8899-c288-6eeb396123b6	Product name	1	20140508
47fd879b-91c5-e1e5-130f-29d082a871ec	Product name	1	20140508
53855190-7124-8179-f018-e792f7c27f28	Product name	1	20140508
6084a4f4-5437-c9a5-caec-5361ee075a59	Product name	1	20140508
7dfac40f-a405-cd2e-7c06-3059ec0e1092	Product name	1	20140508
84fb0b3d-1d72-b672-bc70-2b676a23e7e0	Product name	1	20140508
90c5639a-61b0-88d6-ddcf-21888e94869a	Product name	1	20140508
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877	Product name	1	20140508
96c5169b-5b9d-547d-bf22-d688d91866e4	Product name	1	20140508
b8e0daf1-fb81-290b-c0bf-873be19ef775	Product name	1	20140508
c35d1ac8-8885-2ee1-6c52-5a715b242c00	Product name	1	20140508
c8753a88-edde-8e17-a396-705537b52cee	Product name	1	20140508
cd4f9ae2-1343-ecd2-ce0f-97db0c2b51ce	Product name	1	20140508
cf3a804d-0326-aa22-0142-c184b5657d85	Product name	1	20140508
d83c592c-dd97-4cbf-36ac-13da806684bd	Product name	1	20140508
e01133ad-4dcd-c7f3-454b-2ff569ee160a	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63868-175-26	Pain ReliefChildrens	118 mL in 1 BOTTLE	SUSPENSION	118		5
63868-175-26	Pain ReliefChildrens	1 in 1 BOX	SUSPENSION	1		5

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
63868-175-26	ML - Milliliter	63868-175	ea82d0c5-7e94-4e0e-837f-28f07895e4cb	1	2015-12-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ACETAMINOPHEN	ACTIVE INGREDIENT	362O9ITL9D	PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)]	1
ACETAMINOPHEN	ACTIVE MOIETY	362O9ITL9D	PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)]	1
ACESULFAME POTASSIUM	INACTIVE INGREDIENT	23OV73Q5G9	PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)]	1
ANHYDROUS CITRIC ACID	INACTIVE INGREDIENT	XF417D3PSL	PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)]	1
BUTYLPARABEN	INACTIVE INGREDIENT	3QPI1U3FV8	PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)]	1
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM	INACTIVE INGREDIENT	K679OBS311	PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)]	1
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)]	1
FD&C RED NO. 40	INACTIVE INGREDIENT	WZB9127XOA	PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)]	1
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)]	1
HIGH FRUCTOSE CORN SYRUP	INACTIVE INGREDIENT	XY6UN3QB6S	PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)]	1
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)]	1
SODIUM BENZOATE	INACTIVE INGREDIENT	OJ245FE5EU	PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)]	1
SORBITOL	INACTIVE INGREDIENT	506T60A25R	PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)]	1
XANTHAN GUM	INACTIVE INGREDIENT	TTV12P4NEE	PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63868-175	PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)]	5	Current NDC, Legacy NDC, 2 package rows	20241212_223ffb2b-3ee5-4118-955b-bc4fa4e8a2e6.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 34 of 79 · 1,579 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Headache Relief	ACETAMINOPHEN, ASPIRIN, CAFFEINE	Walmart Inc.	1557bd9b-3e7c-4769-e063-6394a90a9d91	2025-11-04	Warnings	Exact identifier application number: M013
Adult Low Dose Aspirin	ASPIRIN	Rising Pharma Holdings, Inc.	c3c4854e-726e-4926-b044-a5094943c306	2025-11-04	Warnings	Exact identifier application number: M013
Pain Relief	ACETAMINOPHEN	HYVEE INC	3e50b3f6-1e1a-41b9-e063-6394a90abe36	2025-11-03	Warnings	Exact identifier application number: M013
Good Sense Pain Relief	ACETAMINOPHEN	L. Perrigo Company	447de441-7d28-4415-81c5-4fc05622dd05	2025-11-03	Warnings	Exact identifier application number: M013
Children Acetaminophen Oral Solution	ACETAMINOPHEN	VERITYRX. LLC	42a17f54-7851-84fb-e063-6394a90a9ec1	2025-11-02	Warnings	Exact identifier application number: M013
M-PAP	ACETAMINOPHEN	VERITYRX, LLC	42a1a128-a2dd-bbc9-e063-6294a90a4fe1	2025-11-02	Warnings	Exact identifier application number: M013
Physicians Care Aspirin	ASPIRIN	Acme United Corporation	aa67ea3a-2741-7ee0-e053-2a95a90a6485	2025-10-31	Warnings	Exact identifier application number: M013
PhysiciansCare Non Aspirin Extra Strength	ACETAMINOPHEN	Acme United Corporation	c7006775-bd5b-412f-963d-ce5a158216c5	2025-10-31	Warnings	Exact identifier application number: M013
Pain Reliever	ACETAMINOPHEN	Walgreens	f7aa624b-b00c-4fd3-9965-8e4d2b3eb4ba	2025-10-31	Warnings	Exact identifier application number: M013
Extra Strength Acetaminophen	ACETAMINOPHEN	NuCare Pharmaceuticals, Inc.	41affa1a-5aac-7fc0-e063-6394a90a5557	2025-10-30	Warnings	Exact identifier application number: M013
MAPAP Extra Strength	ACETAMINOPHEN	Major Pharmaceuticals	34a95450-3f04-4de4-9113-73e7bd5724a0	2025-10-29	Warnings	Exact identifier application number: M013
GOODNOW PAIN RELIEF	ACETAMINOPHEN	Gobrands, Inc	4d4a78a5-5a88-4f24-b685-c7c6bb5e989e	2025-10-29	Warnings	Exact identifier application number: M013
Sanaflu Xtra	ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE	GRANDALL DISTRIBUTING, LLC	4af8a566-5251-4d46-8692-87a3a0748334	2025-10-28	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	Rising Pharma Holdings, Inc.	f8237772-7656-49fb-b1de-f8fcb5fa55ee	2025-10-28	Warnings	Exact identifier application number: M013
DG Health Pain Relief	ACETAMINOPHEN	Dolgencorp Inc	42f0c87c-7020-4af7-9f6b-3a774137e564	2025-10-24	Warnings	Exact identifier application number: M013
GOODYS Hangover	ASPIRIN AND CAFFEINE	Medtech Products Inc.	0b0067e0-58b0-4581-aa4b-e398c32c559a	2025-10-23	Warnings	Exact identifier application number: M013
GOODYS Extra Strength Headache Mixed Fruit Blast	ACETAMINOPHEN, ASPIRIN, AND CAFFEINE	Medtech Products Inc.	6cb758bf-5a50-46bb-96e7-65b810b12de0	2025-10-23	Warnings	Exact identifier application number: M013
Nyt Time Sleep Caps	DIPHENHYDRAMINE HYDROCHLORIDE	DISCOUNT DRUG MART	e3f4d063-921d-4503-89a6-26cc9c46b4c9	2025-10-23	Warnings	Exact identifier application number: M013
Anacin	ASPRIN AND CAFFEINE	Insight Pharmaceuticals LLC	51ab0ee3-3c94-424d-a30a-2d6c14e3d8ff	2025-10-23	Warnings	Exact identifier application number: M013
Goodys Back and Body Pain	ACETAMINOPHEN AND ASPRIN	Medtech Products Inc.	055d0288-61d4-48bc-b91f-6ecc1969beb8	2025-10-23	Warnings	Exact identifier application number: M013

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
362O9ITL9D	ACETAMINOPHEN	103-90-2	ACETAMINOPHEN

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
307668	acetaminophen 160 MG in 5 mL Oral Suspension	PSN	223ffb2b-3ee5-4118-955b-bc4fa4e8a2e6	5
307668	acetaminophen 32 MG/ML Oral Suspension	SCD	223ffb2b-3ee5-4118-955b-bc4fa4e8a2e6	5
307668	acetaminophen 160 MG per 5 ML Oral Suspension	SY	223ffb2b-3ee5-4118-955b-bc4fa4e8a2e6	5
307668	acetaminophen 320 MG per 10 ML Oral Suspension	SY	223ffb2b-3ee5-4118-955b-bc4fa4e8a2e6	5
307668	acetaminophen 650 MG per 20.3 ML Oral Suspension	SY	223ffb2b-3ee5-4118-955b-bc4fa4e8a2e6	5
307668	acetaminophen 80 MG per 2.5 ML Oral Suspension	SY	223ffb2b-3ee5-4118-955b-bc4fa4e8a2e6	5
307668	APAP 32 MG/ML Oral Suspension	SY	223ffb2b-3ee5-4118-955b-bc4fa4e8a2e6	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63868-175-26	63868017526	1 BOTTLE in 1 BOX (63868-175-26) / 118 mL in 1 BOTTLE	1 bottle	2015-10-31	2021-12-30	No	No	Current