Allergy Multi-Symptom

Product NDC
70677-1004
11-digit product format
706771004
Labeler code
70677
Product ID
70677-1004_24b2650e-08a5-0752-e063-6394a90a4b90
Type
HUMAN OTC DRUG
Nonproprietary name
ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, and PHENYLEPHRINE HYDROCHLORIDE
Dosage form
TABLET, COATED
Route
ORAL
Labeler
STRATEGIC SOURCING SERVICES LLC
Application
M012
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2023-04-25
Substance
ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE
Active strength
325; 2; 5 mg/1; mg/1; mg/1
Pharmacologic classes
Adrenergic alpha1-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-1 Adrenergic Agonist [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
362O9ITL9DACETAMINOPHEN103-90-2ACETAMINOPHEN
V1Q0O9OJ9ZCHLORPHENIRAMINE MALEATE113-92-8CHLORPHENIRAMINE MALEATE
04JA59TNSJPHENYLEPHRINE HYDROCHLORIDE61-76-7PHENYLEPHRINE HYDROCHLORIDE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
70677-1004-1706771004012 BLISTER PACK in 1 CARTON (70677-1004-1) / 12 TABLET, COATED in 1 BLISTER PACK2 blister pack2023-04-25NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
1128B-FST-2023-0425STRATEGIC SOURCING SERVICES LLC2024-10-17HUMAN OTC DRUG LABEL3