allergy childrens
Generic: diphenhydramine hydrochloride
Labeler: h e bDrug Facts
Product Profile
Brand Name
allergy childrens
Generic Name
diphenhydramine hydrochloride
Labeler
h e b
Dosage Form
LIQUID
Routes
Active Ingredients
diphenhydramine hydrochloride 12.5 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
37808-012
Product ID
37808-012_9e60c1a8-4250-402a-8cd8-cb77b9b576ba
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2016-02-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
37808012
Hyphenated Format
37808-012
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
allergy childrens (source: ndc)
Generic Name
diphenhydramine hydrochloride (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 12.5 mg/5mL
Packaging
- 1 BOTTLE, PLASTIC in 1 BOX (37808-012-08) / 237 mL in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9e60c1a8-4250-402a-8cd8-cb77b9b576ba", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1049906"], "spl_set_id": ["ab28cbc4-7a6f-46e9-8616-be78e8cb24fe"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (37808-012-08) / 237 mL in 1 BOTTLE, PLASTIC", "package_ndc": "37808-012-08", "marketing_start_date": "20160229"}], "brand_name": "Allergy Childrens", "product_id": "37808-012_9e60c1a8-4250-402a-8cd8-cb77b9b576ba", "dosage_form": "LIQUID", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "37808-012", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy", "brand_name_suffix": "Childrens", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "12.5 mg/5mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160229", "listing_expiration_date": "20261231"}