Nicorette, Spearmint Burst - Nicotine polacrilex, Spearmint Burst 2 mg / 1 Gum 18 Blister Pack

Reference details for licensed healthcare facility review and verification.

NDC 1100135-0532-14
Product NDC00135-0532
Generic Drug Namenicotine polacrilex, Spearmint Burst
Brand NameNicorette, Spearmint Burst
ManufacturerHaleon US Holdings LLC
Strength2 mg / 1
Dosage FormGum
Drug TypeOral
Package Quantity18 Blister Pack
Package Description18 BLISTER PACK in 1 CARTON (0135-0532-14) / 10 GUM, CHEWING in 1 BLISTER PACK
Active IngredientsNicotine
Marketing CategoryNDA

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NDC snapshot

nicotine polacrilex, Spearmint Burst 2 mg / 1 Gum is tracked under NDC 00135-0532-14 and rolls up into product family 00135-0532. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 18 Blister Pack.
  • Manufacturer: Haleon US Holdings LLC.
  • Dosage form: Gum.
  • Family size: 5 indexed presentations.

Official references

Use official labeling and directory references to confirm presentation details while your team reviews the PRN catalog entry and related sourcing paths.

Alternate presentations in this family

These nearby package-level pages can help healthcare teams compare related packaging or presentation differences inside the same product-NDC family.

Nicorette, Spearmint Burst - Nicotine polacrilex, Spearmint Burst 2 mg / 1 Gum 18 Blister Pack, NDC 00135-0532-14, is a Haleon US Holdings LLC 2 mg / 1 gum presentation packaged as 18 Blister Pack.

NDC search formats

  • Canonical NDC 11: 00135-0532-14
  • Digits-only NDC 11: 00135053214
  • Possible 10-digit display formats: 0135-0532-14 (0135053214), 00135-532-14 (0013553214)

Multiple 10-digit display-format aliases can map to the same stored 11-digit billing NDC, so these are shown as search aliases rather than a single asserted package format.

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