WELL AT WALGREENS BABY ADVANCED HEALING

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: WELL AT WALGREENS BABY ADVANCED HEALING
Generic name: PETROLATUM
Manufacturer: WALGREEN COMPANY
Product type: HUMAN OTC DRUG
SPL set ID: 75067953-4cd8-4fcb-b7b7-dd0d2200642d
SPL ID: 5114ef85-6041-bb94-e063-6294a90a1abc
Version: 4
Effective date: 2026-05-05
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:29:05

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		WELL AT WALGREENS BABY ADVANCED HEALING	openfda.brand_name
generic name		PETROLATUM	openfda.generic_name
manufacturer name		WALGREEN COMPANY	openfda.manufacturer_name
ndc	package	0363-3300-03	openfda.package_ndc
ndc	product	0363-3300	openfda.product_ndc
ndc11	package	00363330003	derived:openfda.package_ndc
spl id		5114ef85-6041-bb94-e063-6294a90a1abc	id
spl set id		75067953-4cd8-4fcb-b7b7-dd0d2200642d	set_id
unii		4T6H12BN9U	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS FOR EXTERNAL USE ONLY WHEN USING THIS PRODUCT AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE THOROUGHLY WITH WATER STOP USE AND ASK A DOCTOR IF CONDITIONS WORSENS. SYMPTOMS LAST MORE THAN 7 DAYS OR CLEAR UP AND OCCUR AGAIN WITHIN A FEW DAYS DO NOT USE ON DEEP PUNCTURE WOUNDS, ANIMAL BITES, SERIOUS BURNS KEEP OUT OF REACH OF CHILDREN IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.