MEDERMA STRETCH MARKS THERAPY

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: MEDERMA STRETCH MARKS THERAPY
Generic name: DIMETHICONE
Manufacturer: L. Perrigo Company
Product type: HUMAN OTC DRUG
SPL set ID: e9366775-e85b-4403-a2c5-12d9fb3cc3fa
SPL ID: e9366775-e85b-4403-a2c5-12d9fb3cc3fa
Version: 1
Effective date: 2026-07-15
Source export date: 2026-09-28
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:48:16

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M016	openfda.application_number
brand name		MEDERMA STRETCH MARKS THERAPY	openfda.brand_name
generic name		DIMETHICONE	openfda.generic_name
manufacturer name		L. Perrigo Company	openfda.manufacturer_name
ndc	package	0113-4053-00	openfda.package_ndc
ndc	product	0113-4053	openfda.product_ndc
ndc11	package	00113405300	derived:openfda.package_ndc
rxcui		244642	openfda.rxcui
rxcui		1483141	openfda.rxcui
spl id		e9366775-e85b-4403-a2c5-12d9fb3cc3fa	id
spl set id		e9366775-e85b-4403-a2c5-12d9fb3cc3fa	set_id
unii		92RU3N3Y1O	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 • Do not get into eyes Stop use and ask a doctor if • Condition worsens • Symptoms last more than 7 days or clear up and occur again within a few days Do not use on • Deep or punctured wounds • Animal bites • Serious burns Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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