mentholatum natural ice original

Generic: dimethicone, octinoxate, octisalate

Labeler: the mentholatum company
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mentholatum natural ice original
Generic Name dimethicone, octinoxate, octisalate
Labeler the mentholatum company
Dosage Form OINTMENT
Routes
TOPICAL
Active Ingredients

dimethicone 10 mg/g, octinoxate 75 mg/g, octisalate 50 mg/g

Manufacturer
The Mentholatum Company

Identifiers & Regulatory

Product NDC 10742-3004
Product ID 10742-3004_292e63d4-99af-0a65-e063-6394a90a3f4f
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 1999-01-19

Pharmacologic Class

Physiologic Effect
skin barrier activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 107423004
Hyphenated Format 10742-3004

Supplemental Identifiers

UNII
92RU3N3Y1O 4Y5P7MUD51 4X49Y0596W
NUI
N0000010282

Packaging Origin

Original Packager
true

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 mentholatum natural ice original (source: ndc)
Generic Name dimethicone, octinoxate, octisalate (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/g
  • 75 mg/g
  • 50 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 BLISTER PACK (10742-3004-2) / 4.2 g in 1 TUBE
  • 1 TUBE in 1 BLISTER PACK (10742-3004-3) / 4.5 g in 1 TUBE
  • 4.5 g in 1 TUBE (10742-3004-4)
  • 4.2 g in 1 TUBE (10742-3004-8)
source: ndc

Packages (4)

10742-3004-2 1 TUBE in 1 BLISTER PACK (10742-3004-2) / 4.2 g in 1 TUBE 10742-3004-3 1 TUBE in 1 BLISTER PACK (10742-3004-3) / 4.5 g in 1 TUBE 10742-3004-4 4.5 g in 1 TUBE (10742-3004-4) 10742-3004-8 4.2 g in 1 TUBE (10742-3004-8)

Ingredients (3)

dimethicone (10 mg/g) octinoxate (75 mg/g) octisalate (50 mg/g)

Linked Drug Pages (1)

Mentholatum Natural Ice Original ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "292e63d4-99af-0a65-e063-6394a90a3f4f", "openfda": {"nui": ["N0000010282"], "unii": ["92RU3N3Y1O", "4Y5P7MUD51", "4X49Y0596W"], "spl_set_id": ["29220eaa-87cb-4ebe-87db-d36288b3a9e4"], "pharm_class_pe": ["Skin Barrier Activity [PE]"], "manufacturer_name": ["The Mentholatum Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BLISTER PACK (10742-3004-2)  / 4.2 g in 1 TUBE", "package_ndc": "10742-3004-2", "marketing_start_date": "20190402"}, {"sample": false, "description": "1 TUBE in 1 BLISTER PACK (10742-3004-3)  / 4.5 g in 1 TUBE", "package_ndc": "10742-3004-3", "marketing_start_date": "19990119"}, {"sample": false, "description": "4.5 g in 1 TUBE (10742-3004-4)", "package_ndc": "10742-3004-4", "marketing_start_date": "19990119"}, {"sample": false, "description": "4.2 g in 1 TUBE (10742-3004-8)", "package_ndc": "10742-3004-8", "marketing_start_date": "20190402"}], "brand_name": "Mentholatum Natural Ice Original", "product_id": "10742-3004_292e63d4-99af-0a65-e063-6394a90a3f4f", "dosage_form": "OINTMENT", "pharm_class": ["Skin Barrier Activity [PE]"], "product_ndc": "10742-3004", "generic_name": "dimethicone, octinoxate, octisalate", "labeler_name": "The Mentholatum Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mentholatum Natural Ice", "brand_name_suffix": "Original", "active_ingredients": [{"name": "DIMETHICONE", "strength": "10 mg/g"}, {"name": "OCTINOXATE", "strength": "75 mg/g"}, {"name": "OCTISALATE", "strength": "50 mg/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19990119", "listing_expiration_date": "20261231"}